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     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
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    <!-- http://purl.obolibrary.org/obo/RO_0000087 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">has role</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/TXPO_0003213 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/TXPO_0003213">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">phospholipidosis dependent molecule  (canonical)</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/TXPO_0004019 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">FLCN(canonical)[Phospholipidosis]</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/TXPO_0003213"/>
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        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">PMID:29848618</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>NCBI-Human-GeneID:201163</oboInOwl:hasDbXref>
        <dc:description>This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]</dc:description>
        <oboInOwl:hasDbXref>NCBI-Mouse-GeneID:216805</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/TXPO_0004043 -->

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    <!-- http://purl.obolibrary.org/obo/TXPO_1000148 -->

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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



