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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <!-- http://purl.obolibrary.org/obo/HP_0030057 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0030057">
        <rdfs:label>Autoimmune antibody positivity</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_6000676 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_6000676">
        <rdfs:label>Anti-von Willebrand factor antibody positivity</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0030057"/>
        <dcterms:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2024-04-01T08:13:26Z</dcterms:date>
        <rdfs:comment>This feature is usually seen in the context of Von Willebrand disease (VWD), the most common inherited bleeding disorder. VWD is caused by deficiency or dysfunction of the multimeric glycoprotein, von Willebrand factor (VWF), and is clinically characterized by excessive mucocutaneous bleeding as well as musculoskeletal bleeding in type 3 VWD, the most severe form. Treatment options include infusion of concentrates of VWF, which in some patients leads to the production of alloantikbodies.</rdfs:comment>
        <ns3:IAO_0000115>The presence of autoantibodies in the serum that react to von Willebrand factor (VWF).</ns3:IAO_0000115>
        <ns3:IAO_0000233 rdf:resource="https://github.com/obophenotype/human-phenotype-ontology/issues/8723"/>
        <dcterms:contributor rdf:resource="https://orcid.org/0000-0002-0736-9199"/>
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