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Namespace Prefixes

PrefixIRI
n7https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
n4http://purl.obolibrary.org/obo/doid#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_12297
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0060039 _:vb50948307 _:vb50948308
rdfs:label
Vogt-Koyanagi-Harada disease
wdrs:describedby
n7:doid.owl
obo:id
DOID:12297
obo:hasDbXref
GARD:7862 NCI:C85218 ICD9CM:364.24 SNOMEDCT_US_2021_09_01:44923005 ICD10CM:H20.82 MESH:D014607 UMLS_CUI:C0042170
obo:hasExactSynonym
Harada's disease uveomeningoencephalitic syndrome Vogt-Koyanagi syndrome
obo:hasOBONamespace
disease_ontology
obo:inSubset
n4:NCIthesaurus
n2:IAO_0000115
An autoimmune disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis.
Subject Item
_:vb50948307
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:SYMP_0019173
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50948308
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004026
owl:someValuesFrom
_:vb50948309
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50948309
rdf:type
owl:Class
owl:intersectionOf
_:vb50948311
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50948310
rdf:first
n2:UBERON_0002384
rdf:rest
rdf:nil
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50948311
rdf:first
n2:UBERON_0000014
rdf:rest
_:vb50948310
wdrs:describedby
n7:doid.owl