<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0007099"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:ns6="http://purl.obolibrary.org/obo/"
     xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
     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:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/"
     xmlns:ns3="http://purl.obolibrary.org/obo/mondo#">
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Annotation properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    <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/mondo#otar"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#excluded_subClassOf"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#exactMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Datatypes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Object Properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- 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>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- http://identifiers.org/hgnc/3661 -->

    <Class rdf:about="http://identifiers.org/hgnc/3661">
        <rdfs:label>FGA</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005240 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005240">
        <rdfs:label>kidney disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0007099 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007099">
        <rdfs:label>familial visceral amyloidosis</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0018634"/>
        <rdfs:subClassOf>
            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/RO_0004003"/>
                <someValuesFrom rdf:resource="http://identifiers.org/hgnc/3661"/>
            </Restriction>
        </rdfs:subClassOf>
        <ns6:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns6:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/8282/amyloidosis-familial-visceral</rdfs:seeAlso>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/amyloidosis_hereditary_systemic_2</ns3:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>amyloidosis familial renal</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>familial renal amyloidosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Ostertag type amyloidosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>amyloidosis, renal</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>amyloidosis, 3 or more types</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:66451004</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>amyloidosis, Ostertag type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>amyloidosis, familial visceral</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C0268389</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>amyloidosis familial visceral</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>familial amyloid nephropathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>amyloidosis, systemic Nonneuropathic</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>hereditary amyloid nephropathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>German type amyloidosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:85450</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:82799</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>amyloidosis 8</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0008282</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C538249</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>hereditary amyloidosis with primary renal involement</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:105200</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007099</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>amyloidosis VIII</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>ICD9:277.39</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200138</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>amyloidosis, familial renal</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>amyloidosis systemic nonneuropathic</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>hereditary renal amyloidosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0050636</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/82799"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C538249"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/66451004"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0268389"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0050636"/>
        <ns3:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005240"/>
        <ns3:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019724"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
        <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_85450"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/105200"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018634 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018634">
        <rdfs:label>hereditary amyloidosis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019724 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019724">
        <rdfs:label>obsolete secondary glomerular disease</rdfs:label>
    </Class>
</rdf:RDF>



<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



