<?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_0004456 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/OAE_0004456">
        <rdfs:label>urinary tract disorder AE</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/OAE_0009106 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/OAE_0009106">
        <rdfs:label>gitelman&#39;s syndrome AE</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/OAE_0004456"/>
        <ns2:OAE_0004334>10062906</ns2:OAE_0004334>
        <ns2:OAE_0001849>gitelman综合征</ns2:OAE_0001849>
        <ns2:IAO_0000117>QY, JX, HY</ns2:IAO_0000117>
        <ns2:IAO_0000119>http://en.volupedia.org/wiki/Gitelman_syndrome</ns2:IAO_0000119>
        <ns2:IAO_0000115>This is an AE which is an autosomal recessive kidney tubule disorder characterized by low blood levels of potassium and magnesium, decreased excretion of calcium in the urine, and elevated blood pH.</ns2:IAO_0000115>
    </Class>
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