<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/UPHENO?iri=http://purl.obolibrary.org/obo/WBPhenotype_0000416"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:ns5="https://w3id.org/semapv/vocab/"
     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:ns4="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://www.geneontology.org/formats/oboInOwl#hasOBONamespace"/>
    <AnnotationProperty rdf:about="https://w3id.org/semapv/vocab/crossSpeciesExactMatch"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasNarrowSynonym"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Datatypes
    //
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    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Object Properties
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    <!-- http://purl.obolibrary.org/obo/UPHENO_0000001 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/UPHENO_0000001">
        <rdfs:label>phenotype affects entity</rdfs:label>
    </ObjectProperty>
    


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

    


    <!-- http://purl.obolibrary.org/obo/GO_0007296 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/GO_0007296">
        <rdfs:label>vitellogenesis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/UPHENO_0049865 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/UPHENO_0049865">
        <rdfs:label>vitellogenesis phenotype</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/WBPhenotype_0000416 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/WBPhenotype_0000416">
        <rdfs:label>yolk synthesis variant</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/UPHENO_0049865"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/WBPhenotype_0001093"/>
        <rdfs:subClassOf>
            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/UPHENO_0000001"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/GO_0007296"/>
            </Restriction>
        </rdfs:subClassOf>
        <ns4:IAO_0000115>Variations in the generation of the nutrient protein produced by intestinal cells and secreted by them into the pseudocoelom, from which it can be shared with other tissues in the body compared to control (Wormatlas).</ns4:IAO_0000115>
        <oboInOwl:hasNarrowSynonym>yolk synthesis abnormal</oboInOwl:hasNarrowSynonym>
        <oboInOwl:id>WBPhenotype:0000416</oboInOwl:id>
        <oboInOwl:hasOBONamespace>C_elegans_phenotype_ontology</oboInOwl:hasOBONamespace>
        <oboInOwl:hasRelatedSynonym>vitellogenin synthesis abnormal</oboInOwl:hasRelatedSynonym>
        <ns5:crossSpeciesExactMatch rdf:resource="http://purl.obolibrary.org/obo/UPHENO_0049865"/>
    </Class>
    


    <!-- 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>
</rdf:RDF>



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



