<?xml version="1.0"?>
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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/OAE_0001849"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000117"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000119"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/OAE_0004334"/>
    


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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/OAE_0000585 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/OAE_0000585">
        <rdfs:label>muscular atrophy AE</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/OAE_0007970 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/OAE_0007970">
        <rdfs:label>peroneal muscular atrophy AE</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/OAE_0000585"/>
        <ns2:OAE_0001849>腓骨肌萎缩症</ns2:OAE_0001849>
        <ns2:IAO_0000117>QY, JX, HY</ns2:IAO_0000117>
        <ns2:OAE_0004334>10034699</ns2:OAE_0004334>
        <ns2:IAO_0000115>This is an AE which is a hereditary motor and sensory neuropathy of the peripheral nervous system characterized by progressive loss of muscle tissue and touch sensation across various parts of the body.</ns2:IAO_0000115>
        <ns2:IAO_0000119>http://en.volupedia.org/wiki/Charcot%E2%80%93Marie%E2%80%93Tooth_disease</ns2:IAO_0000119>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



