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     xmlns:owl="http://www.w3.org/2002/07/owl#"
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    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Annotation properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#disease_grouping"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
    <AnnotationProperty rdf:about="http://purl.org/dc/terms/conformsTo"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#closeMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasNarrowSynonym"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0000053 -->

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        <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>
    </ObjectProperty>
    


    <!-- 
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    //
    // Classes
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003847">
        <rdfs:label>hereditary disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005066 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005066">
        <rdfs:label>metabolic disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019052 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019052">
        <rdfs:label>inborn errors of metabolism</rdfs:label>
        <equivalentClass>
            <Class>
                <intersectionOf rdf:parseType="Collection">
                    <rdf:Description rdf:about="http://purl.obolibrary.org/obo/MONDO_0005066"/>
                    <Restriction>
                        <onProperty rdf:resource="http://purl.obolibrary.org/obo/RO_0000053"/>
                        <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/MONDO_0021152"/>
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                </intersectionOf>
            </Class>
        </equivalentClass>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0003847"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005066"/>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/1483</ns5:IAO_0000233>
        <ns6:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/inherited_metabolic_disorder</ns6:curated_content_resource>
        <oboInOwl:hasExactSynonym>inherited disorders of metabolism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>congenital metabolism disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>congenital metabolic disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:655</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>inherited metabolic disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:86095007</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:6323</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>inherited disorder of metabolism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>hereditary metabolic disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10062018</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0019052</oboInOwl:id>
        <oboInOwl:hasExactSynonym>inborn metabolic disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:733825440</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>inborn errors of metabolism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10058097</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0022508</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D008661</oboInOwl:hasDbXref>
        <oboInOwl:hasNarrowSynonym>rare inherited metabolic disorder</oboInOwl:hasNarrowSynonym>
        <ns5:IAO_0000115>An inherited disorder resulting from an enzyme defect in biochemical and metabolic pathways affecting proteins, fats, carbohydrates metabolism or organelle function.</ns5:IAO_0000115>
        <oboInOwl:hasDbXref>Orphanet:68367</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2100159</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>inborn disorders of metabolism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>inborn error of metabolism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C34816</oboInOwl:hasDbXref>
        <oboInOwl:hasNarrowSynonym>rare inborn errors of metabolism</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasDbXref>UMLS:C0025521</oboInOwl:hasDbXref>
        <rdfs:comment>Note that the ordo class is specifically for rare diseases, but we broaden to be inclusive of HH1</rdfs:comment>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/733825440"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/meddra/10058097"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/meddra/10062018"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/6323"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D008661"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/86095007"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0025521"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_655"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C34816"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <dcterms:conformsTo rdf:resource="http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_68367"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0021152 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021152">
        <rdfs:label>inherited</rdfs:label>
    </Class>
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