<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/EPIO?iri=http://purl.obolibrary.org/obo/DOID_2843"?>
<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:rdfs="http://www.w3.org/2000/01/rdf-schema#"
     xmlns:ns2="http://purl.obolibrary.org/obo/"
     xmlns:ns4="https://bio.scai.fraunhofer.de/ontology/epilepsy#"
     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/IAO_0000412"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="https://bio.scai.fraunhofer.de/ontology/epilepsy#fromILAE"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="https://bio.scai.fraunhofer.de/ontology/epilepsy#fromArticle"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasOBONamespace"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasAlternativeId"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/DOID_2843 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_2843">
        <rdfs:label>long QT syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0001279"/>
        <ns4:fromArticle rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns4:fromArticle>
        <ns4:fromILAE rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns4:fromILAE>
        <oboInOwl:hasDbXref>ORDO:101016</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCI:C34786</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:PS192500</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SNOMEDCT_US_2018_03_01:9651007</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ORDO:768</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D029597</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9CM:426.82</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:6922</oboInOwl:hasDbXref>
        <ns2:IAO_0000115>An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles).</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>CSP2005:4009-0053</oboInOwl:hasDbXref>
        <oboInOwl:id>DOID:2843</oboInOwl:id>
        <oboInOwl:hasDbXref>ICD10CM:I45.81</oboInOwl:hasDbXref>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
        <oboInOwl:hasDbXref>SNOMEDCT_US_2018_03_01:20852007</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS_CUI:C0035828</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>long Q-T syndrome</oboInOwl:hasExactSynonym>
        <rdfs:seeAlso>https://www.epilepsydiagnosis.org/epilepsy-imitators.html#longqt</rdfs:seeAlso>
        <oboInOwl:hasAlternativeId>DOID:4069</oboInOwl:hasAlternativeId>
        <oboInOwl:hasExactSynonym>Romano-Ward syndrome</oboInOwl:hasExactSynonym>
        <rdfs:comment>OMIM mapping confirmed by DO. [SN].</rdfs:comment>
        <oboInOwl:hasDbXref>NCI:C85049</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D008133</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS_CUI:C0023976</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>LQT</oboInOwl:hasExactSynonym>
        <oboInOwl:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/doid#DO_FlyBase_slim"/>
        <oboInOwl:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/doid#NCIthesaurus"/>
        <ns2:IAO_0000412 rdf:resource="http://purl.obolibrary.org/obo/doid.owl"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0001279 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0001279">
        <rdfs:label>Syncope</rdfs:label>
    </Class>
</rdf:RDF>



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



