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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/5476 -->

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        <rdfs:label>IGFBP7</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002311 -->

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        <rdfs:label>retinal vascular disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0013640 -->

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        <rdfs:label>familial retinal arterial macroaneurysm</rdfs:label>
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        <ns6:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6744</ns6:IAO_0000233>
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        <ns6:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6877</ns6:IAO_0000233>
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        <oboInOwl:hasDbXref>MEDGEN:481835</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>SCTID:764452004</oboInOwl:hasDbXref>
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        <oboInOwl:hasExactSynonym>FRAM</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasRelatedSynonym>RAMSVPS</oboInOwl:hasRelatedSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100545 -->

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        <rdfs:label>hereditary neurological disease</rdfs:label>
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