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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004003 -->

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        <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/2682 -->

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        <rdfs:label>DAZ1</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

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        <rdfs:label>hereditary disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015607 -->

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        <rdfs:label>partial chromosome Y deletion</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0042605 -->

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        <rdfs:label>Y chromosome infertility due to DAZ1 deletion</rdfs:label>
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        <oboInOwl:hasRelatedSynonym>male sterility due to Y-chromosome deletions</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>GARD:0000185</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0042605</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>deleted in azoospermia</oboInOwl:hasRelatedSynonym>
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