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Namespace Prefixes

PrefixIRI
n3https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n5http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
dchttp://purl.org/dc/elements/1.1/
obohttp://www.geneontology.org/formats/oboInOwl#
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
_:vb50940424
rdf:type
owl:Axiom
wdrs:describedby
n3:doid.owl
dc:type
n5:ECO_0007636
owl:annotatedProperty
n5:IAO_0000115
owl:annotatedSource
n5:DOID_0080116
owl:annotatedTarget
A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC2 gene on chromosome 6p21.
obo:hasDbXref
url:http://omim.org/entry/615824?search=615824&highlight=615824