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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/12873 -->

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        <rdfs:label>ZIC2</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0012322 -->

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        <rdfs:label>holoprosencephaly 5</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/7693</ns4:IAO_0000233>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/holoprosencephaly_5_2</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>UMLS:C1864827</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0110878</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:609637</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C75460</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0012322</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0024860</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>HPE5</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C566464</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>holoprosencephaly 5</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:355304</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>holoprosencephaly caused by mutation in ZIC2</oboInOwl:hasExactSynonym>
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