<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0019753"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     xml:base="http://www.w3.org/2002/07/owl"
     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:ns4="http://purl.obolibrary.org/obo/mondo#"
     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/"
     xmlns:ns3="http://purl.obolibrary.org/obo/">
    


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

    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <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://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"/>
    <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://purl.obolibrary.org/obo/mondo#ordo_subtype_of_a_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015564 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015564">
        <rdfs:label>Castleman disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019753 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019753">
        <rdfs:label>localized Castleman disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015564"/>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/unicentric_castleman_disease</ns4:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>Unicentric angiofollicular lymph hyperplasia</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:93685</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C115200</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:858176</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>localized Castleman disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>localized Angiofollicular lymphoid hyperplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C3898582</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0006005</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>localised Angiofollicular lymphoid hyperplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Unicentric angiofollicular ganglionic hyperplasia</oboInOwl:hasRelatedSynonym>
        <ns3:IAO_0000115>Localized Castleman disease (LCD) is the most common form of Castleman disease (CD) and it is usually asymptomatic or it may present with enlarged lymph nodes. LCD may be cured by surgical resection.</ns3:IAO_0000115>
        <oboInOwl:id>MONDO:0019753</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>Unicentric Castleman disease</oboInOwl:hasRelatedSynonym>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/858176"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C3898582"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C115200"/>
        <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_subtype_of_a_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_93685"/>
    </Class>
</rdf:RDF>



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



