<?xml version="1.0"?>
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    <!-- http://purl.obolibrary.org/obo/PW_0001627 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/PW_0001627">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">trifunctional protein deficiency pathway</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/PW_0001643"/>
        <oboInOwl:creation_date rdf:datatype="http://www.w3.org/2001/XMLSchema#string">2015-02-19T14:03:09Z</oboInOwl:creation_date>
        <oboInOwl:id rdf:datatype="http://www.w3.org/2001/XMLSchema#string">PW:0001627</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">SMP:00545</oboInOwl:hasRelatedSynonym>
        <ns3:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Trifunctional protein deficiency is caused by alteration in the fatty acid beta degradation pathway. Specifically, mutations in the alpha and beta subunits of the mitochondrial enzyme that catalyzes the last three steps, have been linked to this inherited metabolic condition.</ns3:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/PW_0001643 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/PW_0001643">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">inborn error of lipid metabolism pathway</rdfs:label>
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