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    <rdf:type rdf:resource="&owl;Class" />
    <owl:equivalentClass rdf:nodeID="b1063229312" />
    <rdfs:label>nephronophthisis 9</rdfs:label>
    <rdfs:subClassOf rdf:nodeID="b1063229316" />
    <rdfs:subClassOf rdf:resource="&obo;MONDO_0019005" />
    <ns3:IAO_0000412 rdf:resource="&obo;mondo.owl" />
    <obo:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/mondo#nord_rare" />
    <obo:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/mondo#rare" />
    <obo:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/mondo#gard_rare" />
    <obo:hasDbXref>UMLS:C3151188</obo:hasDbXref>
    <obo:hasDbXref>GARD:0024926</obo:hasDbXref>
    <obo:hasDbXref>MEDGEN:462538</obo:hasDbXref>
    <obo:hasDbXref>DOID:0111120</obo:hasDbXref>
    <obo:hasDbXref>OMIM:613824</obo:hasDbXref>
    <obo:hasExactSynonym>NPHP9</obo:hasExactSynonym>
    <obo:hasExactSynonym>NEK8 nephronophthisis (disease)</obo:hasExactSynonym>
    <obo:hasExactSynonym>nephronophthisis 9</obo:hasExactSynonym>
    <obo:hasExactSynonym>nephronophthisis type 9</obo:hasExactSynonym>
    <obo:hasExactSynonym>nephronophthisis (disease) caused by mutation in NEK8</obo:hasExactSynonym>
    <obo:id>MONDO:0013444</obo:id>
    <ns3:IAO_0000115>Any nephronophthisis in which the cause of the disease is a mutation in the NEK8 gene.</ns3:IAO_0000115>
    <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/nephronophthisis_9</ns5:curated_content_resource>
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    <owl:someValuesFrom rdf:resource="http://identifiers.org/hgnc/13387" />
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<rdf:Description rdf:about="&obo;MONDO_0019005">
    <rdfs:label>nephronophthisis</rdfs:label>
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<rdf:Description rdf:about="&obo;RO_0004003">
    <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <rdfs:label>NEK8</rdfs:label>
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