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Prefix	IRI
n6	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
n8	http://purl.obolibrary.org/obo/doid#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Subject Item: n2:DOID_3770
rdf:type: owl:Class
rdfs:subClassOf: n2:DOID_3082 _:vb50952354 _:vb50952361 _:vb50952362
rdfs:label: pulmonary fibrosis
wdrs:describedby: n6:doid.owl
obo:id: DOID:3770
obo:hasDbXref: MESH:D011658 NCI:C26869 UMLS_CUI:C0034069 SNOMEDCT_US_2021_09_01:155613001
obo:hasExactSynonym: Fibrosis of lung
obo:hasOBONamespace: disease_ontology
obo:inSubset: n8:NCIthesaurus
n2:IAO_0000115: An interstitial lung disease that is characterized by destruction, scarring, and thickening of the interstitial lung tissues and progressive pulmonary function loss in a restrictive pattern, has_symptom progressive shortness of breath, fatigue, and chronic cough, possibly has_material_basis_in exposure to certain chemicals, autoimmune conditions, and radiation.