<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0020693"?>
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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004024 -->

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        <rdfs:label>disease disrupts</rdfs:label>
        <rdfs:label>disease causes disruption of</rdfs:label>
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        <rdfs:label>phosphorylase kinase activity</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002412 -->

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        <rdfs:label>disorder of glycogen metabolism</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005154 -->

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        <rdfs:label>liver disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020693 -->

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        <rdfs:label>glycogen storage disease due to liver phosphorylase kinase deficiency</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4985</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9285</ns4:IAO_0000233>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/glycogen_storage_disease_due_to_liver_phosphorylase_kinase_deficiency</ns5:curated_content_resource>
        <ns4:IAO_0000115>A benign form of phosphorylase kinase deficiency caused by variants in PHKA2 or PHKG2 and characterized by hepatomegaly, growth retardation, and mild delay in motor development during childhood.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0017261</oboInOwl:hasDbXref>
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