<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0010908"?>
<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#otar"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <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#doid_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
    <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_0004024 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004024">
        <rdfs:label>disease disrupts</rdfs:label>
        <rdfs:label>disease causes disruption of</rdfs:label>
    </ObjectProperty>
    


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

    


    <!-- http://purl.obolibrary.org/obo/GO_0042640 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/GO_0042640">
        <rdfs:label>anagen</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0004907 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0004907">
        <rdfs:label>alopecia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0010908 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010908">
        <rdfs:label>loose anagen syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0004907"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0021147"/>
        <rdfs:subClassOf>
            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/RO_0004024"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/GO_0042640"/>
            </Restriction>
        </rdfs:subClassOf>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/loose_anagen_hair_syndrome</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>OMIM:600628</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:98351</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0406468</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:547259783</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D058247</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0003287</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Loose anagen syndrome is a rare benign hair disorder affecting predominantly blond females in childhood and characterized by the presence of hair that can be easily and painlessly pulled out. Most of the hair is in the anagen phase and lacks an external epithelial sheath. Hair grows back quickly and the condition improves spontaneously with aging. Loose anagen hair can be associated with other anomalies, such as coloboma.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>SCTID:238735005</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>loose anagen hair syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0010908</oboInOwl:id>
        <oboInOwl:hasDbXref>DOID:0111702</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:704.8</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:168</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/547259783"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/98351"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D058247"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/238735005"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0406468"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0111702"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
        <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#orphanet_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_168"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/600628"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0021147 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021147">
        <rdfs:label>disorder of development or morphogenesis</rdfs:label>
    </Class>
</rdf:RDF>



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



