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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/doid#DO_rare_slim">
        <rdfs:label>DO_rare_slim</rdfs:label>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0002452 -->

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        <rdfs:label>has symptom</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_0050526 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_0050526">
        <rdfs:label xml:lang="en">Gamstorp-Wohlfart syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_225"/>
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        <oboInOwl:hasDbXref>MIM:137200</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:12353</oboInOwl:hasDbXref>
        <ns4:IAO_0000115 xml:lang="en">A syndrome characterized by progressive weakness and atrophy of muscles in feet, legs and hands. In some patients the syndrome also causes decreased sensitivity to touch, heat or cold, particularly in the lower arms or legs.</ns4:IAO_0000115>
        <rdfs:comment xml:lang="en">OMIM mapping confirmed by DO. [SN].</rdfs:comment>
        <oboInOwl:hasExactSynonym xml:lang="en">autosomal recessive neuromyotonia and axonal neuropathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
        <oboInOwl:hasExactSynonym xml:lang="en">myokymia, myotonia and muscle wasting</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/DOID_225 -->

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        <rdfs:label xml:lang="en">syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/SYMP_0000363 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/SYMP_0000363">
        <rdfs:label>progressive weakness</rdfs:label>
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