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<data xmlns="http://www.aopkb.org/aop-xml">
  <chemical id="ae78671b-d83a-4bef-b5c6-a2d60d2da046">
    <casrn>81-81-2</casrn>
    <jchem-inchi-key>PJVWKTKQMONHTI-UHFFFAOYNA-N</jchem-inchi-key>
    <indigo-inchi-key>PJVWKTKQMONHTI-UHFFFAOYSA-N</indigo-inchi-key>
    <preferred-name>Warfarin</preferred-name>
    <synonyms>
      <synonym>Coumadin</synonym>
      <synonym>2H-1-Benzopyran-2-one, 4-hydroxy-3-(3-oxo-1-phenylbutyl)-</synonym>
      <synonym>(.+-.)-Warfarin</synonym>
      <synonym>(.+-.)-Warfarin-alcohol</synonym>
      <synonym>(RS)-Warfarin</synonym>
      <synonym>1-(4'-Hydroxy-3'-coumarinyl)-1-phenyl-3-butanone</synonym>
      <synonym>3-(1'-Phenyl-2'-acetylethyl)-4-hydroxycoumarin</synonym>
      <synonym>3-(α-Acetonylbenzyl)-4-hydroxycoumarin</synonym>
      <synonym>3-(α-Phenyl-β-acetylethyl)-4-hydroxycoumarin</synonym>
      <synonym>3-(α-Phenyl-β-acetylethyl)-4-hydroxy-coumarin</synonym>
      <synonym>4-Hydroxy-3-(3-oxo-1-phenylbutyl)-2H-1-benzopyran-2-one</synonym>
      <synonym>4-Hydroxy-3-(3-oxo-1-phenylbutyl)-2H-chromen-2-one</synonym>
      <synonym>Athrombine-K</synonym>
      <synonym>BENZOPYRAN(2H-1)-2-ONE, 4-HYDROXY-3-(3-OXO-1- PHENYLBUTYL)-</synonym>
      <synonym>Brumolin</synonym>
      <synonym>Coumafen</synonym>
      <synonym>Coumafene</synonym>
      <synonym>Coumaphen</synonym>
      <synonym>Coumarin, 3-(α-acetonylbenzyl)-4-hydroxy-</synonym>
      <synonym>Coumefene</synonym>
      <synonym>Dethmor</synonym>
      <synonym>DL-3-(α-Acetonylbenzyl)-4-hydroxycoumarin</synonym>
      <synonym>Kumader</synonym>
      <synonym>Kumatox</synonym>
      <synonym>NSC 59813</synonym>
      <synonym>rac-Warfarin</synonym>
      <synonym>Ratron G</synonym>
      <synonym>Rodafarin</synonym>
      <synonym>Rodafarin C</synonym>
      <synonym>Temus W</synonym>
      <synonym>Vampirinip II</synonym>
      <synonym>Vampirinip III</synonym>
      <synonym>W.A.R.F. 42</synonym>
      <synonym>WARF compound 42</synonym>
      <synonym>warfarina</synonym>
      <synonym>Warfarine</synonym>
      <synonym>Zoocoumarin</synonym>
    </synonyms>
    <dsstox-id>DTXSID5023742</dsstox-id>
  </chemical>
  <chemical id="8184da18-fd32-4d3e-b6b1-610145860320">
    <casrn>81-82-3</casrn>
    <jchem-inchi-key>DEKWZWCFHUABHE-UHFFFAOYNA-N</jchem-inchi-key>
    <indigo-inchi-key>DEKWZWCFHUABHE-UHFFFAOYSA-N</indigo-inchi-key>
    <preferred-name>Coumachlor</preferred-name>
    <dsstox-id>DTXSID8041797</dsstox-id>
  </chemical>
  <chemical id="f7bf8bea-a0be-400a-a243-088d0950b84d">
    <casrn>5836-29-3</casrn>
    <jchem-inchi-key>ULSLJYXHZDTLQK-UHFFFAOYNA-N</jchem-inchi-key>
    <indigo-inchi-key>ULSLJYXHZDTLQK-UHFFFAOYSA-N</indigo-inchi-key>
    <preferred-name>Coumatetralyl</preferred-name>
    <dsstox-id>DTXSID8041799</dsstox-id>
  </chemical>
  <chemical id="9f237d65-3b4f-4caf-b246-f32234d895b4">
    <casrn>3691-35-8</casrn>
    <jchem-inchi-key>UDHXJZHVNHGCEC-UHFFFAOYNA-N</jchem-inchi-key>
    <indigo-inchi-key>UDHXJZHVNHGCEC-UHFFFAOYSA-N</indigo-inchi-key>
    <preferred-name>Chlorophacinone</preferred-name>
    <synonyms>
      <synonym>1H-Indene-1,3(2H)-dione, 2-[(4-chlorophenyl)phenylacetyl]-</synonym>
      <synonym>1,3-Indandione, 2-[(p-chlorophenyl)phenylacetyl]-</synonym>
      <synonym>1H-Indene-1,3(2H)-dione, 2-[2-(4-chlorophenyl)-2-phenylacetyl]-</synonym>
      <synonym>2-[(4-Chlorophenyl)phenylacetyl]-1H-indene-1,3-(2H)-dione</synonym>
      <synonym>2-[(p-Chlorophenyl)phenylacetyl]-1,3-indandione</synonym>
      <synonym>2-[2-Phenyl-2-(4-chlorophenyl)acetyl]-1,3-indandione</synonym>
      <synonym>2-Acetyl-2-(p-chlorophenyl)-2-phenylindan-1,3-dione</synonym>
      <synonym>2-Phenyl-p-chlorophenylacetyl-1,3-indandione</synonym>
      <synonym>Chlorodiphacinone</synonym>
      <synonym>Chlorophacinon</synonym>
      <synonym>Chlorphacinone</synonym>
      <synonym>Chlorphenacone</synonym>
      <synonym>clorofacinona</synonym>
      <synonym>Liphadione</synonym>
      <synonym>Raticide</synonym>
      <synonym>Raticide-Caid</synonym>
      <synonym>Redentin</synonym>
    </synonyms>
    <dsstox-id>DTXSID2032348</dsstox-id>
  </chemical>
  <chemical id="65e9f368-0ea2-4428-9a32-584ef1841c7a">
    <casrn>82-66-6</casrn>
    <jchem-inchi-key>JYGLAHSAISAEAL-UHFFFAOYSA-N</jchem-inchi-key>
    <indigo-inchi-key>JYGLAHSAISAEAL-UHFFFAOYSA-N</indigo-inchi-key>
    <preferred-name>Diphacinone</preferred-name>
    <dsstox-id>DTXSID4032378</dsstox-id>
  </chemical>
  <chemical id="c5a0bd35-011b-41a6-99c1-0a20c611fef5">
    <casrn>83-26-1</casrn>
    <jchem-inchi-key>RZKYEQDPDZUERB-UHFFFAOYSA-N</jchem-inchi-key>
    <indigo-inchi-key>RZKYEQDPDZUERB-UHFFFAOYSA-N</indigo-inchi-key>
    <preferred-name>Pindone</preferred-name>
    <synonyms>
      <synonym>1H-Indene-1,3(2H)-dione, 2-(2,2-dimethyl-1-oxopropyl)-</synonym>
      <synonym>2-Pivalyl-1,3-indandione</synonym>
      <synonym>Pival</synonym>
    </synonyms>
    <dsstox-id>DTXSID1025930</dsstox-id>
  </chemical>
  <biological-object id="f9906735-3fb8-455d-b9a6-0cc70990150a">
    <source-id>PR:000007299</source-id>
    <source>PR</source>
    <name>prothrombin</name>
  </biological-object>
  <biological-object id="c3b603d1-fe1e-4fa6-9d5f-40ad7e63be53">
    <source-id>PR:P70375</source-id>
    <source>PR</source>
    <name>coagulation factor VII (mouse)</name>
  </biological-object>
  <biological-object id="e729eb39-ccee-4dc9-9e11-2a99c70a47ec">
    <source-id>PR:P16294</source-id>
    <source>PR</source>
    <name>coagulation factor IX (mouse)</name>
  </biological-object>
  <biological-object id="eb9ab590-eb18-4e25-9759-4e77264f66ae">
    <source-id>PR:O88947</source-id>
    <source>PR</source>
    <name>coagulation factor X (mouse)</name>
  </biological-object>
  <biological-object id="80597ee8-8b31-4612-aada-4bde61b332fb">
    <source-id>CHEBI:33284</source-id>
    <source>CHEBI</source>
    <name>nutrient</name>
  </biological-object>
  <biological-object id="16397190-639e-4e3a-adc1-478b0827cc43">
    <source-id>D001779</source-id>
    <source>MESH</source>
    <name>blood coagulation factors</name>
  </biological-object>
  <biological-object id="0932885c-5a10-4b75-bc21-5eb6ca5e276b">
    <source-id>CHEBI:28384</source-id>
    <source>CHEBI</source>
    <name>vitamin K</name>
  </biological-object>
  <biological-object id="1881bd16-5e4d-4208-8409-caa64a16a7b3">
    <source-id>PR:000004191</source-id>
    <source>PR</source>
    <name>androgen receptor</name>
  </biological-object>
  <biological-object id="c0fceeec-c6f8-46b0-af8f-16a366dcf52b">
    <source-id>D064417</source-id>
    <source>MESH</source>
    <name>Vitamin K Epoxide Reductases</name>
  </biological-object>
  <biological-object id="1d82133f-18dc-4897-9c12-289228d2b530">
    <source-id>UBERON:0000062</source-id>
    <source>UBERON</source>
    <name>organ</name>
  </biological-object>
  <biological-object id="afbe8248-403f-40d2-a719-415306439435">
    <source-id>CHEBI:15422</source-id>
    <source>CHEBI</source>
    <name>ATP</name>
  </biological-object>
  <biological-object id="a42b4cad-eaa2-41f1-8d9f-b96958bf995a">
    <source-id>UBERON:0002049</source-id>
    <source>UBERON</source>
    <name>vasculature</name>
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  <biological-object id="0e72cee1-2a16-4cc0-a192-9966520703a8">
    <source-id>PR:000030444</source-id>
    <source>PR</source>
    <name>osteocalcin</name>
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  <biological-object id="96e7b7d1-5c79-433f-87a6-b27d455205c1">
    <source-id>PR:P19788</source-id>
    <source>PR</source>
    <name>matrix Gla protein (mouse)</name>
  </biological-object>
  <biological-process id="92b9c048-5b05-40dd-8350-518006508c87">
    <source-id>GO:0007599</source-id>
    <source>GO</source>
    <name>hemostasis</name>
  </biological-process>
  <biological-process id="d982027f-ea0e-4574-85c4-264800bf7012">
    <source-id>MP:0001914</source-id>
    <source>MP</source>
    <name>hemorrhage</name>
  </biological-process>
  <biological-process id="abe45562-b7bd-48d3-b973-a11a4ccaae56">
    <source-id>GO:0042060</source-id>
    <source>GO</source>
    <name>wound healing</name>
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  <biological-process id="09d06169-f916-4141-8692-3748b1036b1f">
    <source-id>MI:1139</source-id>
    <source>MI</source>
    <name>carboxylation reaction</name>
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  <biological-process id="a1039a51-e3a8-42b5-9742-addea2d870f0">
    <source-id>GO:0006810</source-id>
    <source>GO</source>
    <name>transport</name>
  </biological-process>
  <biological-process id="a7c9f959-5ace-4893-acd3-474f1b17b310">
    <source-id>GO:1990748</source-id>
    <source>GO</source>
    <name>cellular detoxification</name>
  </biological-process>
  <biological-process id="c8287bd3-54e6-4e3c-9f80-42c20deff310">
    <source-id>MP:0001577</source-id>
    <source>MP</source>
    <name>anemia</name>
  </biological-process>
  <biological-process id="59ef7710-900f-44ce-8e1a-31bbb1f7c990">
    <source-id>GO:0042373</source-id>
    <source>GO</source>
    <name>vitamin K metabolic process</name>
  </biological-process>
  <biological-process id="8cb3adf8-6bda-44ad-b280-bab6f1b2e6b0">
    <source-id>GO:0023052</source-id>
    <source>GO</source>
    <name>signaling</name>
  </biological-process>
  <biological-process id="b492cb7f-d3f4-4faf-b0ec-f0aef1003343">
    <source-id>GO:0003824</source-id>
    <source>GO</source>
    <name>catalytic activity</name>
  </biological-process>
  <biological-process id="6aeaef47-4c83-4728-89d7-098faebb4f5e">
    <source-id>MP:0003031</source-id>
    <source>MP</source>
    <name>acidosis</name>
  </biological-process>
  <biological-process id="f59704e3-9bb8-457e-922f-c4e1c3c20e9b">
    <source-id>MP:0010128</source-id>
    <source>MP</source>
    <name>hypovolemia</name>
  </biological-process>
  <biological-process id="ef502e7b-b1db-4395-ad45-689b4cb50cbc">
    <source-id>VT:1000152</source-id>
    <source>VT</source>
    <name>wellness/fitness trait</name>
  </biological-process>
  <biological-process id="91ab70b7-cd61-4757-9447-0fb7f1f07aed">
    <source-id>D009026</source-id>
    <source>MESH</source>
    <name>mortality</name>
  </biological-process>
  <biological-process id="d74309b3-ff19-4dce-948d-2fb5318e7f1f">
    <source-id>PCO:0000008</source-id>
    <source>PCO</source>
    <name>population growth rate</name>
  </biological-process>
  <biological-process id="9915f582-441b-4e32-8682-7e341f354a86">
    <source-id>GO:0006754</source-id>
    <source>GO</source>
    <name>ATP biosynthetic process</name>
  </biological-process>
  <biological-process id="55386acd-d62d-46ee-9afb-0a476a176f64">
    <source-id>GO:0017077</source-id>
    <source>GO</source>
    <name>oxidative phosphorylation uncoupler activity</name>
  </biological-process>
  <biological-process id="bfe955b9-5bc0-405f-a999-655425063c5c">
    <source-id>MP:0000066</source-id>
    <source>MP</source>
    <name>osteoporosis</name>
  </biological-process>
  <biological-process id="465b5587-d6d4-4065-971f-a8b38755d918">
    <source-id>D061205</source-id>
    <source>MESH</source>
    <name>vascular calcification</name>
  </biological-process>
  <biological-process id="bd444cef-4a41-4ebb-a86b-1ca401360409">
    <source-id>GO:0043687</source-id>
    <source>GO</source>
    <name>post-translational protein modification</name>
  </biological-process>
  <biological-action id="28aeea6b-57a9-4b13-9b10-1d25ff62fdfa">
    <source-id>4</source-id>
    <source>WIKI</source>
    <name>abnormal</name>
  </biological-action>
  <biological-action id="02b8819f-f026-46f9-9b0f-993ccf59a951">
    <source-id>1</source-id>
    <source>WIKI</source>
    <name>increased</name>
  </biological-action>
  <biological-action id="4f23ee2a-6131-4fb3-aff1-37e87826aa42">
    <source-id>2</source-id>
    <source>WIKI</source>
    <name>decreased</name>
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  <biological-action id="78d72d2f-60d8-4532-b74e-18cc40635a9b">
    <source-id>3</source-id>
    <source>WIKI</source>
    <name>occurrence</name>
  </biological-action>
  <biological-action id="f7e6821d-9d78-4050-b5f2-58a63a472143">
    <source-id>7</source-id>
    <source>WIKI</source>
    <name>functional change</name>
  </biological-action>
  <stressor id="5827e84a-eb7f-487a-8cd7-c68e82af923e">
    <name>Warfarin</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="ae78671b-d83a-4bef-b5c6-a2d60d2da046" user-term="Warfarin"/>
    </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="41486966-4b7e-42f8-aae8-bc4e5d529c7f">
    <name>coumachlor</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="8184da18-fd32-4d3e-b6b1-610145860320" user-term="coumachlor"/>
    </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="a1e8ce6a-722f-4e0a-9dbd-e9d3a6247b81">
    <name>coumatetralyl</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="f7bf8bea-a0be-400a-a243-088d0950b84d" user-term="coumatetralyl"/>
    </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="d8221f85-ec4d-4255-8949-839155376d2e">
    <name>chlorophacinone</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="9f237d65-3b4f-4caf-b246-f32234d895b4" user-term="chlorophacinone"/>
    </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="8e249457-84bf-4443-aa17-1170674038d6">
    <name>diphacinone</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="65e9f368-0ea2-4428-9a32-584ef1841c7a" user-term="diphacinone"/>
    </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="157edf4f-d884-4b1a-be1a-199f74268106">
    <name>pindone</name>
    <description></description>
    <chemicals>
      <chemical-initiator chemical-id="c5a0bd35-011b-41a6-99c1-0a20c611fef5" user-term="pindone"/>
    </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="8a0303f2-3df0-4a7a-8e0e-dc6735c40a3b">
    <name>3-[3-(4'-bromo[1,1'-biphenyl]-4-yl)-3-hydroxy-1-phenylpropyl]-4-hydroxy-2-benzopyrone</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>
  <taxonomy id="2ecbed52-8fea-4e38-a622-e1781644e801">
    <source-id>WCS_9606</source-id>
    <source>common toxicological species</source>
    <name>humans</name>
  </taxonomy>
  <taxonomy id="d79b5f7d-0c5c-404e-a925-505ce78050c0">
    <source-id>69158</source-id>
    <source>NCBI</source>
    <name>Rodentia spp.</name>
  </taxonomy>
  <taxonomy id="dc3248b9-61cb-41eb-85ff-f278d1a495fc">
    <source-id>WCS_72873</source-id>
    <source>common ecological species</source>
    <name>birds</name>
  </taxonomy>
  <taxonomy id="5f6f9d00-a30c-45ca-989b-843be83b2dc9">
    <source-id>WikiUser_17</source-id>
    <source/>
    <name>mammals</name>
  </taxonomy>
  <key-event id="c6d440c7-4fa4-4a09-8619-e8779e3be9f1">
    <title>Under carboxylated clotting factors will not assemble on cell surfaces to form clot, Failure of secondary hemostasis  </title>
    <short-name>Under carboxylated clotting factors will not assemble on cell surfaces to form clot, Failur</short-name>
    <biological-organization-level>Tissue</biological-organization-level>
    <description></description>
    <measurement-methodology></measurement-methodology>
    <evidence-supporting-taxonomic-applicability></evidence-supporting-taxonomic-applicability>
    <applicability>
    </applicability>
    <biological-events>
      <biological-event process-id="92b9c048-5b05-40dd-8350-518006508c87" action-id="28aeea6b-57a9-4b13-9b10-1d25ff62fdfa"/>
    </biological-events>
    <references></references>
    <source>AOPWiki</source>
    <creation-timestamp>2016-11-29T18:41:29</creation-timestamp>
    <last-modification-timestamp>2016-12-03T16:37:53</last-modification-timestamp>
  </key-event>
  <key-event id="62a84a51-570e-4fae-a298-da6abf9e27f6">
    <title>Failure in vascular repair mechanisms, Unresolved blood loss (hemorrhage)</title>
    <short-name>Failure in vascular repair mechanisms, Unresolved blood loss (hemorrhage)</short-name>
    <biological-organization-level>Organ</biological-organization-level>
    <description></description>
    <measurement-methodology></measurement-methodology>
    <evidence-supporting-taxonomic-applicability></evidence-supporting-taxonomic-applicability>
    <organ-term>
      <source-id>UBERON:0007798</source-id>
      <source>UBERON</source>
      <name>vascular system</name>
    </organ-term>
    <applicability>
    </applicability>
    <biological-events>
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      <biological-event process-id="abe45562-b7bd-48d3-b973-a11a4ccaae56" action-id="28aeea6b-57a9-4b13-9b10-1d25ff62fdfa"/>
    </biological-events>
    <references></references>
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        <evidence>Low</evidence>
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    <applicability>
      <sex>
        <evidence>Not Specified</evidence>
        <sex>Male</sex>
      </sex>
      <sex>
        <evidence>Not Specified</evidence>
        <sex>Female</sex>
      </sex>
      <life-stage>
        <evidence>High</evidence>
        <life-stage>All life stages</life-stage>
      </life-stage>
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        <evidence>High</evidence>
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        <evidence>High</evidence>
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        <evidence>Moderate</evidence>
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      <description></description>
      <applicability>&lt;p&gt;&lt;a href="#Life_Stage_Applicability"&gt;Life Stage Applicability&lt;/a&gt;, &lt;a href="#Taxonomic_Applicability"&gt; Taxonomic Applicability&lt;/a&gt;, &lt;a href="#Sex_Applicability"&gt; Sex Applicability&lt;/a&gt;&lt;br /&gt;
&lt;em&gt;Elaborate on the domains of applicability listed in the summary section above. Specifically, provide the literature supporting, or excluding, certain domains. &lt;/em&gt; Female rodents are less sensitive to ARs than males Female humans are more sensitive ti ARs than males&lt;/p&gt;
</applicability>
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      <weight-of-evidence-summary></weight-of-evidence-summary>
      <known-modulating-factors/>
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    <potential-applications></potential-applications>
    <aop-stressors>
      <aop-stressor stressor-id="5827e84a-eb7f-487a-8cd7-c68e82af923e">
        <evidence>Not Specified</evidence>
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        <evidence>Not Specified</evidence>
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        <evidence>Not Specified</evidence>
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      <aop-stressor stressor-id="8e249457-84bf-4443-aa17-1170674038d6">
        <evidence>Not Specified</evidence>
      </aop-stressor>
      <aop-stressor stressor-id="157edf4f-d884-4b1a-be1a-199f74268106">
        <evidence>Not Specified</evidence>
      </aop-stressor>
      <aop-stressor stressor-id="8a0303f2-3df0-4a7a-8e0e-dc6735c40a3b">
        <evidence>Not Specified</evidence>
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    <references></references>
    <source>AOPWiki</source>
    <creation-timestamp>2016-11-29T18:41:17</creation-timestamp>
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