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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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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://identifiers.org/hgnc/11772 -->

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        <rdfs:label>TGFBR1</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002527 -->

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        <rdfs:label>keratoacanthoma</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007566 -->

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        <rdfs:label>multiple self-healing squamous epithelioma</rdfs:label>
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        <oboInOwl:hasRelatedSynonym>ESS1 (formerly)</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasExactSynonym>MSSE</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>Orphanet:65748</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:5585</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0003090</oboInOwl:hasDbXref>
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        <oboInOwl:hasExactSynonym>self-healing squamous epithelioma type 1</oboInOwl:hasExactSynonym>
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        <oboInOwl:id>MONDO:0007566</oboInOwl:id>
        <oboInOwl:hasExactSynonym>familial primary self-healing squamous epithelioma of the skin, Ferguson-Smith type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Ferguson-Smith syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>NCIT:C4461</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015356 -->

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        <rdfs:label>hereditary neoplastic syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020173 -->

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