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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/1497 -->

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        <rdfs:label>CASK</rdfs:label>
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        <rdfs:label>FG syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0010318 -->

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        <rdfs:label>FG syndrome 4</rdfs:label>
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        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/9925/x-linked-intellectual-disability-with-or-without-nystagmus</rdfs:seeAlso>
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        <oboInOwl:hasDbXref>OMIM:300422</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>CASK-related FG syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>UMLS:C1845546</oboInOwl:hasDbXref>
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        <oboInOwl:id>MONDO:0010318</oboInOwl:id>
        <oboInOwl:hasExactSynonym>FGS4</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_1060192 -->

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        <rdfs:label>CASK-related intellectual disability</rdfs:label>
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