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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasBroadSynonym"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#excluded_from_qc_check"/>
    


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    <!-- http://purl.obolibrary.org/obo/RO_0000053 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0000053">
        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#InverseFunctionalProperty"/>
        <rdfs:label>has characteristic</rdfs:label>
        <rdfs:label xml:lang="en">has characteristic</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/RO_0004003 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004003">
        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
    </ObjectProperty>
    


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    <!-- http://identifiers.org/hgnc/3337 -->

    <Class rdf:about="http://identifiers.org/hgnc/3337">
        <rdfs:label>ADGRE2</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0000006 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0000006">
        <rdfs:label>Autosomal dominant inheritance</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000426 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000426">
        <rdfs:label>autosomal dominant disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0006618 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006618">
        <rdfs:label>vibratory urticaria</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0007447 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007447">
        <rdfs:label>autosomal dominant vibratory urticaria</rdfs:label>
        <equivalentClass>
            <Class>
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                        <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/HP_0000006"/>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100118"/>
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                <someValuesFrom rdf:resource="http://identifiers.org/hgnc/3337"/>
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        <oboInOwl:id>MONDO:0007447</oboInOwl:id>
        <oboInOwl:hasDbXref>OMIM:193050</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0009806</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>DDU</oboInOwl:hasExactSynonym>
        <ns5:IAO_0000115>An autosomal dominant disease characterized by localized hives and systemic manifestations in response to dermal vibration, with coincident degranulation of mast cells and increased histamine levels in serum.</ns5:IAO_0000115>
        <oboInOwl:hasBroadSynonym>angioedema, vibratory</oboInOwl:hasBroadSynonym>
        <oboInOwl:hasExactSynonym>vibratory urticaria, autosomal dominant</oboInOwl:hasExactSynonym>
        <oboInOwl:hasBroadSynonym>vibratory angioedema</oboInOwl:hasBroadSynonym>
        <oboInOwl:hasExactSynonym>dermodistortive urticaria</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>VBU</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C536347</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:238694002</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:493342</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:125630</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:995.1</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C536347"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/238694002"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_493342"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/125630"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100118 -->

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        <rdfs:label>hereditary skin disorder</rdfs:label>
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