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    <!-- http://purl.obolibrary.org/obo/RO_0004003 -->

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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/7881 -->

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        <rdfs:label>NOTCH1</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003803 -->

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        <rdfs:label>aortic valve disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007194 -->

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        <rdfs:label>familial bicuspid aortic valve</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0024523 -->

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        <rdfs:label>aortic valve disease 1</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C3887892</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_1060150 -->

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