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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0000053 -->

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        <rdfs:label xml:lang="en">has characteristic</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000646 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000646">
        <rdfs:label>ovarian benign neoplasm</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017799 -->

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        <rdfs:label>Meigs syndrome</rdfs:label>
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        <oboInOwl:hasExactSynonym>Meigs&#39; syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Demons-Meigs syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0021372</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:6287</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:314451</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A rare syndrome affecting females. It is characterized by pleural effusion, ascites and non-malignant ovarian neoplasm. This syndrome usually follows a benign course. Prognosis is favorable following surgical resection of the ovarian mass.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>icd11.foundation:1050919535</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D008539</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C3223</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10027139</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0025184</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:629.89</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021058 -->

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        <rdfs:label>neoplastic syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021141 -->

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        <rdfs:label>acquired</rdfs:label>
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