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Prefix	IRI
n7	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#
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_8457
rdf:type: owl:Class
rdfs:subClassOf: n2:DOID_5113 _:vb50955776 _:vb50955777 _:vb50955778 _:vb50955779
rdfs:label: pellagra
wdrs:describedby: n7:doid.owl
obo:id: DOID:8457
obo:hasDbXref: SNOMEDCT_US_2021_09_01:267491008 ICD9CM:265.2 MESH:D010383 UMLS_CUI:C0030783 GARD:10014
obo:hasExactSynonym: Niacin deficiency Pellagra Niacin-tryptophan deficiency
obo:hasOBONamespace: disease_ontology
n2:IAO_0000115: A nutritional deficiency disease that is characterized by deficiency of niacin (vitamin B3), has_symptom gastrointestinal disturbance, anorexia, diarrhea, dementia, hallucinations, depression, psychosis, and/or non-specific skin changes, and has_material_basis_in deficiency of niacin, often from inadequate diet, malabsorption, or medication side effects.