<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/HP?iri=http://purl.obolibrary.org/obo/HP_0030130"?>
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     xmlns:owl="http://www.w3.org/2002/07/owl#"
     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    


    <!-- 
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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/HP_0012146 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0012146">
        <rdfs:label>Abnormality of von Willebrand factor</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0030130 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0030130">
        <rdfs:label>Impaired von Willebrand factor collagen binding activity</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0012146"/>
        <oboInOwl:hasDbXref>UMLS:C4022618</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Reduced ability of von Willebrand factor (vWF) to bind collagen. Abnormal response to collagen as manifested by reduced or lacking ability of plasma von WIllebrand Factor to bind collagen. An ELISA-based assay is typically used; the test is sensitive to loss of von Willebrand Factor high molecular weight multimers.</ns3:IAO_0000115>
        <rdfs:comment>This abnormality may be seen in von Willebrand disease type 1, type 2A, type 2B, and type 3.</rdfs:comment>
    </Class>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



