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        <rdfs:label>disease has location</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_0050156 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_0050156">
        <rdfs:label xml:lang="en">idiopathic pulmonary fibrosis</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_3770"/>
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        <ns4:IAO_0000115 xml:lang="en">A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe.</ns4:IAO_0000115>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
        <oboInOwl:hasDbXref>UMLS_CUI:C1800706</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>GARD:8609</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>ICD9CM:516.31</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SNOMEDCT_US_2025_09_01:28168000</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D054990</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym xml:lang="en">FIBROCYSTIC PULMONARY DYSPLASIA</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCI:C35716</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym xml:lang="en">IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL</oboInOwl:hasExactSynonym>
        <rdfs:comment xml:lang="en">OMIM mapping confirmed by DO. [SN].</rdfs:comment>
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        <rdfs:label xml:lang="en">pulmonary fibrosis</rdfs:label>
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        <rdfs:label>autosomal dominant inheritance</rdfs:label>
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        <rdfs:label>Abnormal pulmonary interstitial morphology</rdfs:label>
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