<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/EFO?iri=http://purl.obolibrary.org/obo/MONDO_0007902"?>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0006572 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006572">
        <rdfs:label>lichen planus</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0007902 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007902">
        <rdfs:label>lichen planus, familial</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0006572"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100118"/>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/lichen_planus_familial</ns4:curated_content_resource>
        <oboInOwl:hasDbXref>MEDGEN:372036</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>hereditary lichen planus</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C563624</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:151620</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>An instance of lichen planus that is caused by an inherited modification of the individual&#39;s genome.</ns3:IAO_0000115>
        <oboInOwl:id>MONDO:0007902</oboInOwl:id>
        <oboInOwl:hasExactSynonym>lichen planus, familial</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1835402</oboInOwl:hasDbXref>
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        <skos:exactMatch rdf:resource="https://omim.org/entry/151620"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100118 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100118">
        <rdfs:label>hereditary skin disorder</rdfs:label>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



