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    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0020028">
        <rdfs:label xml:lang="en">autosomal dominant retinitis pigmentosa</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_98657"/>
        <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2021-10-28T07:56:15Z</dc:date>
        <oboInOwl:hasDbXref>Medgen:CN239354</oboInOwl:hasDbXref>
        <dc:creator>zmp</dc:creator>
        <ns3:IAO_0000115>Autosomal dominant retinitis pigmentosa (RP) is an autosomally dominant inherited retinal dystrophy leading to progressive loss of the photoreceptors and retinal pigment epithelium and resulting in blindness usually after several decades.</ns3:IAO_0000115>
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