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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/16446 -->

    <Class rdf:about="http://identifiers.org/hgnc/16446">
        <rdfs:label>CARD14</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005083 -->

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        <rdfs:label>psoriasis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0006547 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006547">
        <rdfs:label>exanthem</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008251 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0008251">
        <rdfs:label>familial pityriasis rubra pilaris</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/3470</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9285</ns5:IAO_0000233>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/pityriasis_rubra_pilaris</ns3:curated_content_resource>
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        <oboInOwl:hasDbXref>MESH:C531784</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Devergie&#39;s disease</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0008251</oboInOwl:id>
        <oboInOwl:hasDbXref>OMIM:173200</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0024612</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:443914</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10035116</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C2930842</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2897</oboInOwl:hasDbXref>
        <oboInOwl:hasBroadSynonym>pityriasis rubra pilaris</oboInOwl:hasBroadSynonym>
        <ns5:IAO_0000115>A rare chronic papulosquamous disorder of unknown etiology characterized by small follicular papules, scaly red-orange patches, and palmoplantar hyperkeratosis, which may progress to plaques or erythroderma. Although most of the cases are sporadic and acquired, a familial form of the disease exists.</ns5:IAO_0000115>
        <oboInOwl:hasExactSynonym>hereditary pityriasis rubra pilaris</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>pityriasis rubra pilaris--familial type</oboInOwl:hasExactSynonym>
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