<?xml version="1.0"?>
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     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
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    <!-- 
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasOBONamespace"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/PW_0000345 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/PW_0000345">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">cerebral arterial diseases pathway</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/PW_0000346 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/PW_0000346">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">CADASIL pathway</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/PW_0000345"/>
        <ns3:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">CADASIL - cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy - a disease of the small cerebral arteries characterized by subcortical stroke and vascular dementia. It is associated with mutations in the Notch3 gene. More than fifty mutations are clustered within the first EGF repeats and involve the gain or loss of a cysteine.</ns3:IAO_0000115>
        <oboInOwl:id rdf:datatype="http://www.w3.org/2001/XMLSchema#string">PW:0000346</oboInOwl:id>
        <oboInOwl:hasOBONamespace rdf:datatype="http://www.w3.org/2001/XMLSchema#string">pathway</oboInOwl:hasOBONamespace>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



