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     xml:base="http://www.w3.org/2002/07/owl"
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     xmlns:owl="http://www.w3.org/2002/07/owl#"
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     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    


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    <!-- http://purl.obolibrary.org/obo/RO_0004003 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004003">
        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
    </ObjectProperty>
    


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    <!-- http://identifiers.org/hgnc/21641 -->

    <Class rdf:about="http://identifiers.org/hgnc/21641">
        <rdfs:label>TSPAN12</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019516 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019516">
        <rdfs:label>exudative vitreoretinopathy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0100484 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100484">
        <rdfs:label>TSPAN12-related vitreoretinopathy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0700231 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0700231">
        <rdfs:label>TSPAN12-related exudative vitreoretinopathy</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6562</ns4:IAO_0000233>
        <oboInOwl:id>MONDO:0700231</oboInOwl:id>
        <ns4:IAO_0000115>Any exudative vitreoretinopathy caused by variants in the TSPAN12 gene.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0026380</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>TSPAN12-related exudative vitreoretinopathy</oboInOwl:hasExactSynonym>
        <rdfs:comment>This term captures the disease spectrum. At the time of creation (January 2024), this term is the ontological parent to only one term, but other clinical disease terms could be added in the future. If no additional ontological children are discovered, it is possible that this term might be merged with its single child. (https://clinicalgenome.org/working-groups/clinical-domain/ocular-cdwg/)</rdfs:comment>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
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