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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0000053 -->

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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#InverseFunctionalProperty"/>
        <rdfs:label>has characteristic</rdfs:label>
        <rdfs:label xml:lang="en">has characteristic</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0000006 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0000006">
        <rdfs:label>Autosomal dominant inheritance</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000426 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000426">
        <rdfs:label>autosomal dominant disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0004579 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0004579">
        <rdfs:label>retinoschisis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008382 -->

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        <rdfs:label>retinoschisis, autosomal dominant</rdfs:label>
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        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/retinoschisis_autosomal_dominant_2</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>MESH:C000598640</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>retinoschisis autosomal dominant</oboInOwl:hasRelatedSynonym>
        <ns4:IAO_0000115>Autosomal dominant form of retinoschisis.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>MEDGEN:357940</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1867235</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:180270</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>autosomal dominant retinoschisis</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019118 -->

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        <rdfs:label>inherited retinal dystrophy</rdfs:label>
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