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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/doid#DO_rare_slim">
        <rdfs:label>DO_rare_slim</rdfs:label>
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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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    <!-- http://purl.obolibrary.org/obo/IDO_0000664 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/IDO_0000664">
        <rdfs:label>has material basis in</rdfs:label>
    </ObjectProperty>
    


    <!-- http://purl.obolibrary.org/obo/RO_0004019 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004019">
        <rdfs:label>disease has basis in</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_0050735 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_0050735">
        <rdfs:label xml:lang="en">X-linked monogenic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_0080015 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_0080015">
        <rdfs:label xml:lang="en">physical disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/DOID_0111862 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_0111862">
        <rdfs:label xml:lang="en">congenital bilateral absence of vas deferens</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_0050735"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_0080015"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_12336"/>
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        </rdfs:subClassOf>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
        <oboInOwl:id>DOID:0111862</oboInOwl:id>
        <oboInOwl:hasDbXref>ORDO:48</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym xml:lang="en">CAVD</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MIM:PS277180</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym xml:lang="en">CBAVD</oboInOwl:hasExactSynonym>
        <skos:exactMatch>MIM:PS277180</skos:exactMatch>
        <ns4:IAO_0000115 xml:lang="en">A male infertility that is characterized by bilateral absence of the vas deferens resulting in obstroctive azoospermia and male infertility.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym xml:lang="en">congenital bilateral agenesis of vas deferens</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">congenital bilateral aplasia of vas deferens</oboInOwl:hasExactSynonym>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/doid#DO_rare_slim"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/DOID_12336 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_12336">
        <rdfs:label xml:lang="en">male infertility</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/GENO_0000936 -->

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        <rdfs:label xml:lang="en">X-linked inheritance</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0001197 -->

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        <rdfs:label>Abnormality of prenatal development or birth</rdfs:label>
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