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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000117"/>
    <AnnotationProperty rdf:about="http://www.ebi.ac.uk/efo/reason_for_obsolescence"/>
    <AnnotationProperty rdf:about="http://www.ebi.ac.uk/efo/obsoleted_in_version"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0100001"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://www.ebi.ac.uk/efo/EFO_1001452 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_1001452">
        <rdfs:label>obsolete_Yellow Nail Syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.w3.org/2002/07/owl#Thing"/>
        <deprecated rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</deprecated>
        <oboInOwl:hasDbXref>ICD10:L60.5</oboInOwl:hasDbXref>
        <ns2:IAO_0000117>Sirarat Sarntivijai</ns2:IAO_0000117>
        <ns2:IAO_0100001>http://purl.obolibrary.org/obo/MONDO_0007921</ns2:IAO_0100001>
        <ns5:reason_for_obsolescence>Replaced by Mondo term MONDO_0007921, with which this term was previously merged. Use: http://purl.obolibrary.org/obo/MONDO_0007921</ns5:reason_for_obsolescence>
        <oboInOwl:hasDbXref>MedDRA:10048244</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ORDO:Orphanet_662</oboInOwl:hasDbXref>
        <ns5:obsoleted_in_version>3.88.0</ns5:obsoleted_in_version>
        <ns2:IAO_0000115>A rare condition characterized by the presence of yellow nails, LYMPHEDEMA, and/or PLEURAL EFFUSION with respiratory tract involvement. Abnormal lymphatic network may play a role in its etiology. Occasionally inherited, yellow nail syndrome mostly is sporadic without apparent family history.</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>DOID:0050468</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:153300</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIt:C85238</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D056684</oboInOwl:hasDbXref>
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