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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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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>
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    <!-- http://identifiers.org/hgnc/6654 -->

    <Class rdf:about="http://identifiers.org/hgnc/6654">
        <rdfs:label>LMX1B</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0009724 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009724">
        <rdfs:label>nail-patella-like renal disease</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/4521</ns4:IAO_0000233>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/focal_segmental_glomerulosclerosis_10</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>ICD9:756.89</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C537228</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0403548</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A severe nephropathy characterized by renal dysfunction, proteinuria, edema and microscopic haematuria. It has been described in three brothers, two of which died from end-stage renal insufficiency.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>nail-patella-like renal disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:256020</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2613</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>focal segmental glomerulosclerosis 10</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>nail patella like renal disease</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:140789</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Salcedo syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:236527004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0000321</oboInOwl:hasDbXref>
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        <rdfs:label>inherited kidney disorder</rdfs:label>
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