<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0010869"?>
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     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/MONDO_0001627 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0001627">
        <rdfs:label>dementia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003425 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003425">
        <rdfs:label>ophthalmoplegia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0010869 -->

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        <rdfs:label>motor neuron disease with dementia and ophthalmoplegia</rdfs:label>
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        <oboInOwl:hasExactSynonym>motor neuron disease with dementia and ophthalmoplegia</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>MESH:C563954</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1838253</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0024759</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:600333</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0024257 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0024257">
        <rdfs:label>hereditary motor neuron disease</rdfs:label>
    </Class>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



