<?xml version="1.0" encoding="UTF-8"?>
<data xmlns="http://www.aopkb.org/aop-xml">
  <chemical id="0d94d026-cc61-4cca-84de-62122514a70e">
    <casrn>298-46-4</casrn>
    <jchem-inchi-key>FFGPTBGBLSHEPO-UHFFFAOYSA-N</jchem-inchi-key>
    <indigo-inchi-key>FFGPTBGBLSHEPO-UHFFFAOYSA-N</indigo-inchi-key>
    <preferred-name>Carbamazepine</preferred-name>
    <synonyms>
      <synonym>Carbazepine</synonym>
      <synonym>5H-Dibenz[b,f]azepine-5-carboxamide</synonym>
      <synonym>5-Carbamoyl-5H-dibenz[b,f]azepine</synonym>
      <synonym>5H-Dibenzo [b,f] azepine-5-carboxamide</synonym>
      <synonym>Amizepin</synonym>
      <synonym>Calepsin</synonym>
      <synonym>Carbamazepen</synonym>
      <synonym>Carbamazepin</synonym>
      <synonym>carbamazepina</synonym>
      <synonym>Carbatrol</synonym>
      <synonym>Carbelan</synonym>
      <synonym>Finlepsin</synonym>
      <synonym>Geigy 32883</synonym>
      <synonym>Karbamazepin</synonym>
      <synonym>Karbelex</synonym>
      <synonym>Karberol</synonym>
      <synonym>Neurotol</synonym>
      <synonym>Neurotop</synonym>
      <synonym>NSC 169864</synonym>
      <synonym>Stazepine</synonym>
      <synonym>Tegretal</synonym>
      <synonym>Tegretol</synonym>
      <synonym>Tegretol XR</synonym>
      <synonym>Telesmin</synonym>
      <synonym>Timonil</synonym>
    </synonyms>
    <dsstox-id>DTXSID4022731</dsstox-id>
  </chemical>
  <chemical id="66cf5da6-4421-4333-90bf-2b1747b60ed1">
    <casrn>97240-79-4</casrn>
    <jchem-inchi-key>KJADKKWYZYXHBB-XBWDGYHZSA-N</jchem-inchi-key>
    <indigo-inchi-key>KJADKKWYZYXHBB-XBWDGYHZSA-N</indigo-inchi-key>
    <preferred-name>Topiramate</preferred-name>
    <synonyms>
      <synonym>β-D-Fructopyranose, 2,3:4,5-bis-O-(1-methylethylidene)-, sulfamate</synonym>
      <synonym>2,3:4,5-Bis-O-(1-methylethylidene) β-D-fructopyranose sulfamate</synonym>
      <synonym>Epitoma</synonym>
      <synonym>Epitomax</synonym>
      <synonym>Topamac</synonym>
      <synonym>Topamax</synonym>
      <synonym>Topimax</synonym>
      <synonym>Topomax</synonym>
      <synonym>β-D-Fructopyranose, 2,3:4,5-bis-O-(1-methylethylidene)-, 1-sulfamate</synonym>
    </synonyms>
    <dsstox-id>DTXSID8023688</dsstox-id>
  </chemical>
  <chemical id="8208313d-b28b-45ad-ab3f-85335071a68d">
    <casrn>1951-25-3</casrn>
    <jchem-inchi-key>IYIKLHRQXLHMJQ-UHFFFAOYSA-N</jchem-inchi-key>
    <indigo-inchi-key>IYIKLHRQXLHMJQ-UHFFFAOYSA-N</indigo-inchi-key>
    <preferred-name>Amiodarone</preferred-name>
    <synonyms>
      <synonym>Methanone, (2-butyl-3-benzofuranyl)[4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl]-</synonym>
      <synonym>2-Butyl-3-[3,5-diiodo-4-(2-diethylaminoethoxy)benzoyl]benzofuran</synonym>
      <synonym>2-Butyl-3-benzofuranyl p-[(2-diethylamino)ethoxy]-m,m-diiodophenyl ketone</synonym>
      <synonym>2-n-Butyl-3',5'-diiodo-4'-N-diethylaminoethoxy-3-benzoylbenzofuran</synonym>
      <synonym>Amidorone</synonym>
      <synonym>Amiodaron</synonym>
      <synonym>amiodarona</synonym>
      <synonym>Ancaron</synonym>
      <synonym>Ketone, 2-butyl-3-benzofuranyl 4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl</synonym>
      <synonym>Sedacoron</synonym>
      <synonym>Sedacorone</synonym>
    </synonyms>
    <dsstox-id>DTXSID7022592</dsstox-id>
  </chemical>
  <chemical id="66e534e6-572a-499c-a303-9236a04b256e">
    <casrn>68291-97-4</casrn>
    <jchem-inchi-key>UBQNRHZMVUUOMG-UHFFFAOYSA-N</jchem-inchi-key>
    <indigo-inchi-key>UBQNRHZMVUUOMG-UHFFFAOYSA-N</indigo-inchi-key>
    <preferred-name>Zonisamide</preferred-name>
    <synonyms>
      <synonym>1,2-Benzisoxazole-3-methanesulfonamide</synonym>
    </synonyms>
    <dsstox-id>DTXSID9046023</dsstox-id>
  </chemical>
  <chemical id="c0a6b11b-e03a-41d1-9644-3dcf2f9a8ce3">
    <casrn>137-58-6</casrn>
    <jchem-inchi-key>NNJVILVZKWQKPM-UHFFFAOYSA-N</jchem-inchi-key>
    <indigo-inchi-key>NNJVILVZKWQKPM-UHFFFAOYSA-N</indigo-inchi-key>
    <preferred-name>Lidocaine</preferred-name>
    <synonyms>
      <synonym>Acetamide, 2-(diethylamino)-N-(2,6-dimethylphenyl)-</synonym>
      <synonym>2-(Diethylamino)-2',6'-acetoxylidide</synonym>
      <synonym>2-(Diethylamino)-N-(2,6-dimethylphenyl)acetamide</synonym>
      <synonym>2',6'-Acetoxylidide, 2-(diethylamino)-</synonym>
      <synonym>2-Diethylamino-2,6'-acetoxylidide</synonym>
      <synonym>Anbesol</synonym>
      <synonym>Anestacon</synonym>
      <synonym>Aritmal</synonym>
      <synonym>Cuivasil</synonym>
      <synonym>Dalcaine</synonym>
      <synonym>Duncaine</synonym>
      <synonym>ELA-Max</synonym>
      <synonym>Esracaine</synonym>
      <synonym>Isicaina</synonym>
      <synonym>Isicaine</synonym>
      <synonym>Jetocaine</synonym>
      <synonym>Leostesin</synonym>
      <synonym>Lida-Mantle</synonym>
      <synonym>Lidocadren</synonym>
      <synonym>Lidocain</synonym>
      <synonym>lidocaina</synonym>
      <synonym>Lidoderm</synonym>
      <synonym>Lignocaine</synonym>
      <synonym>Maricaine</synonym>
      <synonym>NSC 40030</synonym>
      <synonym>Remicaine</synonym>
      <synonym>Rucaina</synonym>
      <synonym>Solarcaine</synonym>
      <synonym>Solcain</synonym>
      <synonym>Trachisan</synonym>
      <synonym>Xycaine</synonym>
      <synonym>Xylestesin</synonym>
      <synonym>Xylocain</synonym>
      <synonym>XYLOCAINE</synonym>
      <synonym>Xylocitin</synonym>
      <synonym>α-Diethylamino-2,6-acetoxylidide</synonym>
    </synonyms>
    <dsstox-id>DTXSID1045166</dsstox-id>
  </chemical>
  <biological-object id="0a8dc5b9-5bdb-43ba-a311-1e1e349776bb">
    <source-id>PR:000002095</source-id>
    <source>PR</source>
    <name>sodium channel protein type 1 subunit alpha</name>
  </biological-object>
  <biological-object id="eecf6213-73b8-4862-8c7c-a2610273506d">
    <source-id>CHEBI:29101</source-id>
    <source>CHEBI</source>
    <name>sodium(1+)</name>
  </biological-object>
  <biological-object id="e59410ba-1bb1-4ca2-9962-72bb4013667a">
    <source-id>CHEBI:16865</source-id>
    <source>CHEBI</source>
    <name>gamma-aminobutyric acid</name>
  </biological-object>
  <biological-process id="6787403e-2432-4893-945b-2b6543e7ef42">
    <source-id>GO:0019871</source-id>
    <source>GO</source>
    <name>sodium channel inhibitor activity</name>
  </biological-process>
  <biological-process id="56b68f36-6558-4679-ad5e-229b3dd9834e">
    <source-id>GO:0023052</source-id>
    <source>GO</source>
    <name>signaling</name>
  </biological-process>
  <biological-process id="04dd38f9-5bfc-4d93-881f-958073a7b551">
    <source-id>GO:0006810</source-id>
    <source>GO</source>
    <name>transport</name>
  </biological-process>
  <biological-action id="2d83bacd-a698-40ec-b2cb-12335108feb9">
    <source-id>2</source-id>
    <source>WIKI</source>
    <name>decreased</name>
  </biological-action>
  <stressor id="7c8f926b-8b7a-44af-850b-a2a4c66c9750">
    <name>Carbamazepine</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="0d94d026-cc61-4cca-84de-62122514a70e" user-term="Carbamazepine"/>
    </chemicals>
    <exposure-characterization></exposure-characterization>
    <creation-timestamp>2016-11-29T18:42:27</creation-timestamp>
    <last-modification-timestamp>2016-11-29T18:42:27</last-modification-timestamp>
  </stressor>
  <stressor id="ce1916a4-66f9-4d7d-8c04-cf32c59b030a">
    <name>Topiramate</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="66cf5da6-4421-4333-90bf-2b1747b60ed1" user-term="Topiramate"/>
    </chemicals>
    <exposure-characterization></exposure-characterization>
    <creation-timestamp>2016-11-29T18:42:27</creation-timestamp>
    <last-modification-timestamp>2016-11-29T18:42:27</last-modification-timestamp>
  </stressor>
  <stressor id="0554804c-8159-4562-b187-a1eb10d5040e">
    <name>Tetrodotoxin</name>
    <description></description>
    <exposure-characterization></exposure-characterization>
    <creation-timestamp>2016-11-29T18:42:27</creation-timestamp>
    <last-modification-timestamp>2016-11-29T18:42:27</last-modification-timestamp>
  </stressor>
  <stressor id="fdc5c0c0-65e9-4617-a756-ee72ed865060">
    <name>Amiodarone</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="8208313d-b28b-45ad-ab3f-85335071a68d" user-term="Amiodarone"/>
    </chemicals>
    <exposure-characterization></exposure-characterization>
    <creation-timestamp>2016-11-29T18:42:27</creation-timestamp>
    <last-modification-timestamp>2016-11-29T18:42:27</last-modification-timestamp>
  </stressor>
  <stressor id="0416dafc-4e4a-438f-bf3c-5e61b2ffb488">
    <name>Phenytoin</name>
    <description></description>
    <exposure-characterization></exposure-characterization>
    <creation-timestamp>2016-11-29T18:42:27</creation-timestamp>
    <last-modification-timestamp>2016-11-29T18:42:27</last-modification-timestamp>
  </stressor>
  <stressor id="cb49916a-3212-4a88-824f-41fed89c3dc4">
    <name>Valproate</name>
    <description></description>
    <exposure-characterization></exposure-characterization>
    <creation-timestamp>2016-11-29T18:42:27</creation-timestamp>
    <last-modification-timestamp>2016-11-29T18:42:27</last-modification-timestamp>
  </stressor>
  <stressor id="8f1f2025-0f94-4821-a749-4be18d4e7b49">
    <name>Zonisamide</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="66e534e6-572a-499c-a303-9236a04b256e" user-term="Zonisamide"/>
    </chemicals>
    <exposure-characterization></exposure-characterization>
    <creation-timestamp>2016-11-29T18:42:27</creation-timestamp>
    <last-modification-timestamp>2016-11-29T18:42:27</last-modification-timestamp>
  </stressor>
  <stressor id="97693aed-794e-48b9-813a-6faae0bafe5d">
    <name>Lidocaine</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="c0a6b11b-e03a-41d1-9644-3dcf2f9a8ce3" user-term="Lidocaine"/>
    </chemicals>
    <exposure-characterization></exposure-characterization>
    <creation-timestamp>2016-11-29T18:42:27</creation-timestamp>
    <last-modification-timestamp>2016-11-29T18:42:27</last-modification-timestamp>
  </stressor>
  <key-event id="d88e2623-9f4b-4214-83ec-f66586425f28">
    <title>Inhibition, sodium channel</title>
    <short-name>Inhibition, sodium channel</short-name>
    <biological-organization-level>Molecular</biological-organization-level>
    <description>&lt;p&gt;Voltage-gated sodium channels consist of an alpha subunit and auxiliary beta subunits.  The alpha subunit is the ion pore-forming component of the channel and is organized into four homologous domains (I- IV), each with six trans-membrane alpha helices (S1-S6).  Between the S5 and S6  segments, there is a pore loop which is a primary target for anti-epileptic drugs.   The segments between S5 and S6  in each of the four domains create extracellular pore loops.  Amino acid  changes in the poor loops within domains II and IV determine if the ion channel is sensitive to sodium or calcium ions. Anti-epileptic, anti-arrhythmic and anesthetics all may bind this same site, but their action may be voltage-specific. For example, phenytoin is an ineffective block of hyperpolarized (e.g., -100mV) sodium channels, but is  more effective at blocking progressively depolarized potentials (e.g., -80 to -30 mV).
&lt;/p&gt;</description>
    <measurement-methodology>&lt;p&gt;&lt;em&gt;
Voltage-clamp recordings of sodium currents is a general means of detection.  ToxCast assay NVS_IC_rNaCh_site 2 also measures binding to the sodium channel receptor.
&lt;/em&gt;
&lt;/p&gt;</measurement-methodology>
    <evidence-supporting-taxonomic-applicability></evidence-supporting-taxonomic-applicability>
    <cell-term>
      <source-id>CL:0000255</source-id>
      <source>CL</source>
      <name>eukaryotic cell</name>
    </cell-term>
    <applicability>
    </applicability>
    <biological-events>
      <biological-event object-id="0a8dc5b9-5bdb-43ba-a311-1e1e349776bb" process-id="6787403e-2432-4893-945b-2b6543e7ef42" action-id="2d83bacd-a698-40ec-b2cb-12335108feb9"/>
      <biological-event object-id="0a8dc5b9-5bdb-43ba-a311-1e1e349776bb" process-id="56b68f36-6558-4679-ad5e-229b3dd9834e" action-id="2d83bacd-a698-40ec-b2cb-12335108feb9"/>
    </biological-events>
    <references>&lt;p&gt;Ragsdale, D.S. and Avoli, M. 1998. Sodium channels as molecular targets for antiepileptic drugs. Brain Research Reviews 26:16-28.
&lt;/p&gt;&lt;p&gt;Pless, S.A., Galpin, J.D., Frankel, A., and Ahern, C.A. 2011. Molecular basis for class Ib anti-arrhythmic inhibition of cardiac sodium channels. Nat Commun 2:351.
&lt;/p&gt;</references>
    <source>AOPWiki</source>
    <creation-timestamp>2016-11-29T18:41:25</creation-timestamp>
    <last-modification-timestamp>2017-09-16T10:15:48</last-modification-timestamp>
  </key-event>
  <key-event id="580a58e8-b6db-4fe7-b950-c7a7c1613dde">
    <title>Decreased, sodium conductance 2</title>
    <short-name>Decreased, sodium conductance 2</short-name>
    <biological-organization-level>Cellular</biological-organization-level>
    <description></description>
    <measurement-methodology></measurement-methodology>
    <evidence-supporting-taxonomic-applicability></evidence-supporting-taxonomic-applicability>
    <applicability>
    </applicability>
    <biological-events>
      <biological-event object-id="eecf6213-73b8-4862-8c7c-a2610273506d" process-id="04dd38f9-5bfc-4d93-881f-958073a7b551" action-id="2d83bacd-a698-40ec-b2cb-12335108feb9"/>
    </biological-events>
    <references></references>
    <source>AOPWiki</source>
    <creation-timestamp>2016-11-29T18:41:30</creation-timestamp>
    <last-modification-timestamp>2016-12-03T16:37:53</last-modification-timestamp>
  </key-event>
  <key-event id="4a360757-33df-4fe0-bc35-31e00516dfd9">
    <title>Decreased, GABA release</title>
    <short-name>Decreased, GABA release</short-name>
    <biological-organization-level>Cellular</biological-organization-level>
    <description></description>
    <measurement-methodology></measurement-methodology>
    <evidence-supporting-taxonomic-applicability></evidence-supporting-taxonomic-applicability>
    <applicability>
    </applicability>
    <biological-events>
      <biological-event object-id="e59410ba-1bb1-4ca2-9962-72bb4013667a" process-id="04dd38f9-5bfc-4d93-881f-958073a7b551" action-id="2d83bacd-a698-40ec-b2cb-12335108feb9"/>
    </biological-events>
    <references></references>
    <source>AOPWiki</source>
    <creation-timestamp>2016-11-29T18:41:30</creation-timestamp>
    <last-modification-timestamp>2016-12-03T16:37:53</last-modification-timestamp>
  </key-event>
  <key-event-relationship id="87311c1a-0243-4b25-81b8-d18677b63f55">
    <title>
      <upstream-id>d88e2623-9f4b-4214-83ec-f66586425f28</upstream-id>
      <downstream-id>580a58e8-b6db-4fe7-b950-c7a7c1613dde</downstream-id>
    </title>
    <description></description>
    <evidence-collection-strategy/>
    <weight-of-evidence>
      <value></value>
      <biological-plausibility></biological-plausibility>
      <emperical-support-linkage></emperical-support-linkage>
      <uncertainties-or-inconsistencies></uncertainties-or-inconsistencies>
    </weight-of-evidence>
    <known-modulating-factors/>
    <quantitative-understanding>
      <description></description>
      <response-response-relationship/>
      <time-scale/>
      <feedforward-feedback-loops/>
    </quantitative-understanding>
    <applicability>
    </applicability>
    <evidence-supporting-taxonomic-applicability></evidence-supporting-taxonomic-applicability>
    <references>#&lt;Reference::ActiveRecord_Associations_CollectionProxy:0x00007b42e9c4ed28&gt;</references>
    <source>AOPWiki</source>
    <creation-timestamp>2016-11-29T18:41:37</creation-timestamp>
    <last-modification-timestamp>2016-12-03T16:38:06</last-modification-timestamp>
  </key-event-relationship>
  <key-event-relationship id="874052f3-47e3-4a3c-a079-70caaebcc84c">
    <title>
      <upstream-id>580a58e8-b6db-4fe7-b950-c7a7c1613dde</upstream-id>
      <downstream-id>4a360757-33df-4fe0-bc35-31e00516dfd9</downstream-id>
    </title>
    <description></description>
    <evidence-collection-strategy/>
    <weight-of-evidence>
      <value></value>
      <biological-plausibility></biological-plausibility>
      <emperical-support-linkage></emperical-support-linkage>
      <uncertainties-or-inconsistencies></uncertainties-or-inconsistencies>
    </weight-of-evidence>
    <known-modulating-factors/>
    <quantitative-understanding>
      <description></description>
      <response-response-relationship/>
      <time-scale/>
      <feedforward-feedback-loops/>
    </quantitative-understanding>
    <applicability>
    </applicability>
    <evidence-supporting-taxonomic-applicability></evidence-supporting-taxonomic-applicability>
    <references>#&lt;Reference::ActiveRecord_Associations_CollectionProxy:0x00007b42e9ce3478&gt;</references>
    <source>AOPWiki</source>
    <creation-timestamp>2016-11-29T18:41:37</creation-timestamp>
    <last-modification-timestamp>2016-12-03T16:38:06</last-modification-timestamp>
  </key-event-relationship>
  <aop id="002bd62f-47fb-463a-bd30-9e61b7e425e8">
    <title>Sodium channel (Nav1.1) inhibition leading to population decline</title>
    <short-name>Nav1.1 inhibition to population decline</short-name>
    <point-of-contact>Evgeniia Kazymova</point-of-contact>
    <authors>&lt;p&gt;Kellie Fay&lt;/p&gt;
</authors>
    <coaches>
    </coaches>
    <external_links>
    </external_links>
    <status>
      <wiki-license>BY-SA</wiki-license>
    </status>
    <oecd-project>1.29</oecd-project>
    <handbook-version>1.0</handbook-version>
    <abstract></abstract>
    <molecular-initiating-event key-event-id="d88e2623-9f4b-4214-83ec-f66586425f28">
      <evidence-supporting-chemical-initiation></evidence-supporting-chemical-initiation>
    </molecular-initiating-event>
    <key-events>
      <key-event key-event-id="580a58e8-b6db-4fe7-b950-c7a7c1613dde"/>
      <key-event key-event-id="4a360757-33df-4fe0-bc35-31e00516dfd9"/>
    </key-events>
    <key-event-relationships>
      <relationship id="87311c1a-0243-4b25-81b8-d18677b63f55">
        <adjacency>adjacent</adjacency>
        <quantitative-understanding-value>Not Specified</quantitative-understanding-value>
        <evidence>Not Specified</evidence>
      </relationship>
      <relationship id="874052f3-47e3-4a3c-a079-70caaebcc84c">
        <adjacency>adjacent</adjacency>
        <quantitative-understanding-value>Not Specified</quantitative-understanding-value>
        <evidence>Not Specified</evidence>
      </relationship>
    </key-event-relationships>
    <applicability>
    </applicability>
    <overall-assessment>
      <description></description>
      <applicability></applicability>
      <key-event-essentiality-summary></key-event-essentiality-summary>
      <weight-of-evidence-summary></weight-of-evidence-summary>
      <known-modulating-factors/>
      <quantitative-considerations></quantitative-considerations>
    </overall-assessment>
    <potential-applications></potential-applications>
    <references></references>
    <source>AOPWiki</source>
    <creation-timestamp>2016-11-29T18:41:17</creation-timestamp>
    <last-modification-timestamp>2023-09-25T16:26:55</last-modification-timestamp>
  </aop>
  <vendor-specific id="318c2f70-515c-4382-9ada-0d1509242800" name="AopWiki" version="2026-04-04 00:53:11 +0000">
    <biological-process-reference id="6787403e-2432-4893-945b-2b6543e7ef42" aop-wiki-id="28750"/>
    <biological-process-reference id="56b68f36-6558-4679-ad5e-229b3dd9834e" aop-wiki-id="10077"/>
    <biological-process-reference id="04dd38f9-5bfc-4d93-881f-958073a7b551" aop-wiki-id="14461"/>
    <biological-action-reference id="2d83bacd-a698-40ec-b2cb-12335108feb9" aop-wiki-id="2"/>
    <chemical-reference id="0d94d026-cc61-4cca-84de-62122514a70e" aop-wiki-id="22731"/>
    <chemical-reference id="66cf5da6-4421-4333-90bf-2b1747b60ed1" aop-wiki-id="23688"/>
    <chemical-reference id="8208313d-b28b-45ad-ab3f-85335071a68d" aop-wiki-id="22592"/>
    <chemical-reference id="66e534e6-572a-499c-a303-9236a04b256e" aop-wiki-id="46023"/>
    <chemical-reference id="c0a6b11b-e03a-41d1-9644-3dcf2f9a8ce3" aop-wiki-id="45166"/>
    <stressor-reference id="7c8f926b-8b7a-44af-850b-a2a4c66c9750" aop-wiki-id="92"/>
    <stressor-reference id="ce1916a4-66f9-4d7d-8c04-cf32c59b030a" aop-wiki-id="93"/>
    <stressor-reference id="0554804c-8159-4562-b187-a1eb10d5040e" aop-wiki-id="94"/>
    <stressor-reference id="fdc5c0c0-65e9-4617-a756-ee72ed865060" aop-wiki-id="95"/>
    <stressor-reference id="0416dafc-4e4a-438f-bf3c-5e61b2ffb488" aop-wiki-id="96"/>
    <stressor-reference id="cb49916a-3212-4a88-824f-41fed89c3dc4" aop-wiki-id="97"/>
    <stressor-reference id="8f1f2025-0f94-4821-a749-4be18d4e7b49" aop-wiki-id="98"/>
    <stressor-reference id="97693aed-794e-48b9-813a-6faae0bafe5d" aop-wiki-id="99"/>
    <biological-object-reference id="0a8dc5b9-5bdb-43ba-a311-1e1e349776bb" aop-wiki-id="66515"/>
    <biological-object-reference id="eecf6213-73b8-4862-8c7c-a2610273506d" aop-wiki-id="59311"/>
    <biological-object-reference id="e59410ba-1bb1-4ca2-9962-72bb4013667a" aop-wiki-id="43826"/>
    <key-event-reference id="d88e2623-9f4b-4214-83ec-f66586425f28" aop-wiki-id="584"/>
    <key-event-reference id="580a58e8-b6db-4fe7-b950-c7a7c1613dde" aop-wiki-id="1176"/>
    <key-event-reference id="4a360757-33df-4fe0-bc35-31e00516dfd9" aop-wiki-id="1179"/>
    <key-event-relationship-reference id="87311c1a-0243-4b25-81b8-d18677b63f55" aop-wiki-id="1242"/>
    <key-event-relationship-reference id="874052f3-47e3-4a3c-a079-70caaebcc84c" aop-wiki-id="1244"/>
    <aop-reference id="002bd62f-47fb-463a-bd30-9e61b7e425e8" aop-wiki-id="197"/>
  </vendor-specific>
</data>
