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Prefix	IRI
n3	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n4	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: n4:DOID_8857
rdf:type: owl:Class
rdfs:subClassOf: n4:DOID_0060032 _:vb50956133 _:vb50956134 _:vb50956135 _:vb50956136 _:vb50956137
rdfs:label: lupus erythematosus
wdrs:describedby: n3:doid.owl
obo:id: DOID:8857
obo:hasDbXref: SNOMEDCT_US_2021_09_01:200936003 ICD9CM:695.4 ICD10CM:L93 UMLS_CUI:C0409974 NCI:C27153
obo:hasExactSynonym: lupus
obo:hasOBONamespace: disease_ontology
obo:inSubset: n8:NCIthesaurus
n4:IAO_0000115: An autoimmune disease that is characterized by a constellation of findings that include elevated antibodies to nuclear antigens, antiphospholipids, low complement levels, ulcers, non-scarring alopecia, renal or neurologic damage, and low white blood cell and platelet counts, has_symptom rashes, fatigue, arthritis, hair loss, seizures, and symptoms related to affected organs.