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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/7907 -->

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        <rdfs:label>NPHP3</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0009966 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009966">
        <rdfs:label>NPHP3-related Meckel-like syndrome</rdfs:label>
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        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/4665/dandy-walker-cyst-with-renal-hepatic-pancreatic-dysplasia</rdfs:seeAlso>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/meckel_syndrome_type_7</ns4:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>Dandy-Walker cyst with renal-hepatic-pancreatic dysplasia</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>UMLS:C2673885</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:382217</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>renal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Meckel syndrome, type 7</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Meckel-like syndrome type 1</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Goldston syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>MKS7</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Meckel syndrome type 7</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0004665</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>NPHP3-related Meckel-like syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:267010</oboInOwl:hasDbXref>
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        <oboInOwl:hasRelatedSynonym>renal-hepatic-pancreatic dysplasia with Dandy-Walker cyst</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>PMID:18371931</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C537756</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:3032</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0070121</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018921 -->

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        <rdfs:label>Meckel syndrome</rdfs:label>
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        <rdfs:label>central nervous system malformation</rdfs:label>
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        <rdfs:label>hereditary neurological disease</rdfs:label>
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