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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"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://www.ebi.ac.uk/efo/EFO_1000672 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_1000672">
        <rdfs:label>obsolete_Bloch-Sulzberger syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.w3.org/2002/07/owl#Thing"/>
        <ns5:organizational_class rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns5:organizational_class>
        <deprecated rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</deprecated>
        <ns5:reason_for_obsolescence>Duplication of Orphanet term
Use: Orphanet_464 Label: Incontinentia pigmenti</ns5:reason_for_obsolescence>
        <ns2:IAO_0000115>a genetic disorder that affects the skin, hair, teeth, nails, and central nervous system.</ns2:IAO_0000115>
        <oboInOwl:hasExactSynonym>Incontinentia pigmenti syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Wikipedia:Incongenita_pigmenti</oboInOwl:hasDbXref>
        <ns2:IAO_0000117>Sirarat Sarntivijai</ns2:IAO_0000117>
        <ns2:IAO_0100001>http://www.orpha.net/ORDO/Orphanet_464</ns2:IAO_0100001>
        <ns5:obsoleted_in_version>2.100</ns5:obsoleted_in_version>
        <oboInOwl:hasExactSynonym>Incontinentia pigmenti</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>melanoblastosis cutis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>nevus pigmentosus systematicus</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Bloch-Siemens syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:12305</oboInOwl:hasDbXref>
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