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    <!-- 
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    //
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#disease_grouping"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004020 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004020">
        <rdfs:label>disease has basis in dysfunction of</rdfs:label>
    </ObjectProperty>
    


    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004029">
        <rdfs:label>disease has feature</rdfs:label>
    </ObjectProperty>
    


    <!-- 
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    <!-- http://purl.obolibrary.org/obo/HP_0001251 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0001251">
        <rdfs:label>Ataxia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000437 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000437">
        <rdfs:label>cerebellar ataxia</rdfs:label>
        <equivalentClass>
            <Class>
                <intersectionOf rdf:parseType="Collection">
                    <rdf:Description rdf:about="http://purl.obolibrary.org/obo/MONDO_0100308"/>
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                        <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/UBERON_0002037"/>
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                </intersectionOf>
            </Class>
        </equivalentClass>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005395"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0022687"/>
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        <rdfs:subClassOf>
            <Restriction>
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                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/HP_0001251"/>
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        </rdfs:subClassOf>
        <rdfs:subClassOf>
            <Restriction>
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                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/UBERON_0002037"/>
            </Restriction>
        </rdfs:subClassOf>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/8301</ns4:IAO_0000233>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/rare_ataxia</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>DOID:0050753</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0000437</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>cerebellar dysmetria</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C0007758</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:85102008</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200882</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:102002</oboInOwl:hasDbXref>
        <rdfs:comment>In ORDO this is called rare ataxia, we rename as ataxia since all forms are individually rare</rdfs:comment>
        <oboInOwl:hasRelatedSynonym>ataxia</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>spinocerebellar degeneration</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>cerebellar dysmetrias</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>ataxia, cerebellar</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>ataxias, cerebellar</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0019816</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:1200037</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>cerebellar ataxias</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:334.3</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2100238</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ataxia syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C82341</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D002524</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:849</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A neurological syndrome characterized by clumsy and uncoordinated movement of the limbs, trunk, and cranial muscles. It results from pathology in the cerebellum and its connections, or in the proprioceptive sensory pathways.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>spinocerebellar ataxia</oboInOwl:hasExactSynonym>
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        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D002524"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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        <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_102002"/>
        <ns5:curated_content_resource rdf:resource="https://search.clinicalgenome.org/kb/conditions/MONDO:0000437"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005395 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005395">
        <rdfs:label>movement disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0022687 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0022687">
        <rdfs:label>cerebellar degeneration</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0100308 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100308">
        <rdfs:label>atactic disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/UBERON_0002037 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/UBERON_0002037">
        <rdfs:label>cerebellum</rdfs:label>
    </Class>
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