<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/UPHENO?iri=http://purl.obolibrary.org/obo/WBPhenotype_0001347"?>
<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: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://www.geneontology.org/formats/oboInOwl#hasOBONamespace"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasNarrowSynonym"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/WBPhenotype_0001093 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/WBPhenotype_0001093">
        <rdfs:label>intestinal physiology variant</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/WBPhenotype_0001347 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/WBPhenotype_0001347">
        <rdfs:label>intestinal calcium signaling variant</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/WBPhenotype_0001093"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/WBPhenotype_0002170"/>
        <oboInOwl:id>WBPhenotype:0001347</oboInOwl:id>
        <ns3:IAO_0000115>Any variation in the series of molecular signals in which an intestinal cell uses calcium ions to convert an extracellular signal into a response, compared to control.</ns3:IAO_0000115>
        <oboInOwl:hasOBONamespace>C_elegans_phenotype_ontology</oboInOwl:hasOBONamespace>
        <oboInOwl:hasNarrowSynonym>intestinal calcium signaling abnormal</oboInOwl:hasNarrowSynonym>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/WBPhenotype_0002170 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/WBPhenotype_0002170">
        <rdfs:label>calcium mediated signaling variant</rdfs:label>
    </Class>
</rdf:RDF>



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



