<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0017453"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:ns5="http://purl.obolibrary.org/obo/mondo#"
     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/"
     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/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <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#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"/>
    


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

    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Object Properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- http://purl.obolibrary.org/obo/RO_0014001 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0014001">
        <rdfs:label>disease has infectious agent</rdfs:label>
    </ObjectProperty>
    


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

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016511 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016511">
        <rdfs:label>infectious embryofetopathy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0017453 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017453">
        <rdfs:label>fetal parvovirus syndrome</rdfs:label>
        <equivalentClass>
            <Class>
                <intersectionOf rdf:parseType="Collection">
                    <rdf:Description rdf:about="http://purl.obolibrary.org/obo/MONDO_0016511"/>
                    <Restriction>
                        <onProperty rdf:resource="http://purl.obolibrary.org/obo/RO_0014001"/>
                        <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/NCBITaxon_10798"/>
                    </Restriction>
                </intersectionOf>
            </Class>
        </equivalentClass>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016511"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0025371"/>
        <rdfs:subClassOf>
            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/RO_0014001"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/NCBITaxon_10798"/>
            </Restriction>
        </rdfs:subClassOf>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/fetal_parvovirus_syndrome</ns5:curated_content_resource>
        <oboInOwl:id>MONDO:0017453</oboInOwl:id>
        <ns4:IAO_0000115>Foetal parvovirus syndrome is a foetopathy likely to occur when a pregnant woman is infected by parvovirus B19. In adults, the virus causes a butterfly erythema infectiosum (also called Fifth Disease; &#39;slapped cheek disease&#39;) and flu-like symptoms with symmetric polyarthralgias, which usually do not warrant prenatal diagnosis.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>mother-to-child transmission of parvovirus syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Parvovirus antenatal infection</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:648536096</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C2931167</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0004236</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>fifth disease</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Human parvovirus B19 infectious embryofetopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C536301</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Maternofetal infection by parvovirus</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:715197005</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:295</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Human parvovirus B19 caused infectious embryofetopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Parvovirus B19 antenatal infection</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:443992</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/648536096"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/443992"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C536301"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/715197005"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C2931167"/>
        <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#ordo_malformation_syndrome"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_295"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0025371 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0025371">
        <rdfs:label>Parvoviridae infectious disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/NCBITaxon_10798 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/NCBITaxon_10798">
        <rdfs:label>Human parvovirus B19</rdfs:label>
    </Class>
</rdf:RDF>



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



