<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/OAE?iri=http://purl.obolibrary.org/obo/OAE_0005581"?>
<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: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/OAE_0001849"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000117"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000119"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/OAE_0004334"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/OAE_0000539 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/OAE_0000539">
        <rdfs:label>paralysis AE</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/OAE_0005581 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/OAE_0005581">
        <rdfs:label>familial periodic paralysis AE</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/OAE_0000539"/>
        <ns2:OAE_0004334>10016208</ns2:OAE_0004334>
        <ns2:IAO_0000115>This is an AE which is a group of rare genetic diseases that lead to weakness or paralysis from common triggers such as cold, heat, high carbohydrate meals, not eating, stress or excitement and physical activity of any kind.</ns2:IAO_0000115>
        <ns2:IAO_0000119>http://en.volupedia.org/wiki/Periodic_paralysis</ns2:IAO_0000119>
        <ns2:IAO_0000117>QY, JX, HY</ns2:IAO_0000117>
        <ns2:OAE_0001849>家族性周期性麻痹</ns2:OAE_0001849>
    </Class>
</rdf:RDF>



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



