<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/EFO?iri=http://purl.obolibrary.org/obo/MONDO_0011150"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:ns5="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:ORDO="http://www.orpha.net/ORDO/"
     xmlns:ns2="http://purl.obolibrary.org/obo/mondo#"
     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


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

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


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

    


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

    


    <!-- 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_0011150 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011150">
        <rdfs:label>acroosteolysis-keloid-like lesions-premature aging syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0003847"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019303"/>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/1567</ns5:IAO_0000233>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/premature_aging_syndrome_penttinen_type</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>Orphanet:363665</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>premature aging syndrome Penttinen type</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0004276</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:400936</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C536653</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0011150</oboInOwl:id>
        <oboInOwl:hasDbXref>UMLS:C1866182</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>premature ageing syndrome, Penttinen type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>PENTT</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>premature aging syndrome, Penttinen type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>progeroid syndrome, Penttinen type</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Penttinen-aula syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:601812</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>premature ageing syndrome Penttinen type</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>prematurely aged appearance, delayed bone maturation, acro-osteolysis, and brachydactyly</oboInOwl:hasRelatedSynonym>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/400936"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C536653"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C1866182"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015333"/>
        <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_363665"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/601812"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015333 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015333">
        <rdfs:label>progeroid syndrome</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019303 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019303">
        <rdfs:label>premature aging syndrome</rdfs:label>
    </Class>
    


    <!-- http://www.orpha.net/ORDO/Orphanet_363665 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_363665">
        <rdfs:label>obsolete_acroosteolysis-keloid-like lesions-premature aging syndrome</rdfs:label>
    </Class>
</rdf:RDF>



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



