<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0015900"?>
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     xml:base="http://www.w3.org/2002/07/owl"
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     xmlns:owl="http://www.w3.org/2002/07/owl#"
     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
     xmlns:xsd="http://www.w3.org/2001/XMLSchema#"
     xmlns:skos="http://www.w3.org/2004/02/skos/core#"
     xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#"
     xmlns:obo="http://purl.obolibrary.org/obo/"
     xmlns:ns4="http://purl.obolibrary.org/obo/mondo#"
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     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
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    //
    // Annotation properties
    //
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    <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.obolibrary.org/obo/mondo#curated_content_resource"/>
    <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://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#exactMatch"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    


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    // Datatypes
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    <!-- 
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    //
    // Object Properties
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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004029">
        <rdfs:label>disease has feature</rdfs:label>
    </ObjectProperty>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
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    <!-- http://purl.obolibrary.org/obo/HP_0004319 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0004319">
        <rdfs:label>Decreased circulating aldosterone concentration</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005495 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005495">
        <rdfs:label>adrenal gland disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015900 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015900">
        <rdfs:label>hypoaldosteronism disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005495"/>
        <rdfs:subClassOf>
            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/RO_0004029"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/HP_0004319"/>
            </Restriction>
        </rdfs:subClassOf>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/rare_hypoaldosteronism</ns4:curated_content_resource>
        <oboInOwl:hasDbXref>NANDO:2100132</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>hypoaldosteronism</oboInOwl:hasRelatedSynonym>
        <rdfs:comment>Editor note: we place the GARD class here as it is implicitly rare</rdfs:comment>
        <oboInOwl:hasDbXref>SCTID:60086000</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:181419</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D006994</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0020228</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:208996</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>rare hypoaldosteronism</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0015900</oboInOwl:id>
        <oboInOwl:hasDbXref>UMLS:C0857899</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/208996"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D006994"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/60086000"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0857899"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#disease_grouping"/>
        <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"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_181419"/>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



