<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0000030"?>
<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#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#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://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#clingen"/>
    <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"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#should_conform_to"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000030 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000030">
        <rdfs:label>familial sleep-related hypermotor epilepsy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0017704"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100631"/>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/3891</ns3:IAO_0000233>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/8455</ns3:IAO_0000233>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9285</ns3:IAO_0000233>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9740</ns3:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.epilepsydiagnosis.org/syndrome/adnfle-overview.html</rdfs:seeAlso>
        <oboInOwl:hasDbXref>UMLS:C5577629</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:1004734747</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0060681</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>An instance of sleep-related hypermotor epilepsy that is caused by an inherited genomic modification in an individual.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>MEDGEN:1865268</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0000030</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0011918</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:600513</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C579932</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>famillial SHE</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0022703</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C3696898</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:777188</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>autosomal dominant nocturnal frontal lobe epilepsy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:698021005</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ADNFLE</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:98784</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>familial sleep-related hypermotor epilepsy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>epilepsy, nocturnal frontal lobe, familial</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>familial sleep-related hyperkinetic epilepsy</oboInOwl:hasExactSynonym>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/1004734747"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/1865268"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/777188"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C579932"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/698021005"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C3696898"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C5577629"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0060681"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#clingen"/>
        <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"/>
        <ns4:should_conform_to rdf:resource="http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_98784"/>
        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS600513"/>
        <ns4:curated_content_resource rdf:resource="https://search.clinicalgenome.org/kb/conditions/MONDO:0000030"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0017704 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017704">
        <rdfs:label>familial partial epilepsy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0100631 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100631">
        <rdfs:label>sleep-related hypermotor epilepsy</rdfs:label>
    </Class>
</rdf:RDF>



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



