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Namespace Prefixes

PrefixIRI
n7https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3http://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#
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
n3:DOID_0080111
rdf:type
owl:Class
rdfs:subClassOf
_:vb50940413 n3:DOID_0111139
rdfs:label
mitochondrial complex III deficiency nuclear type 1
wdrs:describedby
n7:doid.owl
obo:id
DOID:0080111
obo:hasDbXref
OMIM:124000
obo:hasOBONamespace
disease_ontology
n3:IAO_0000115
A mitochondrial complex III deficiency characterized by onset at birth of lactic acidosis, hypotonia, hypoglycemia, failure to thrive, encephalopathy, and delayed psychomotor development and that has_material_basis_in homozygous or compound heterozygous mutation in the nuclear-encoded BCS1L gene on chromosome 2q35.
Subject Item
_:vb50940413
rdf:type
owl:Restriction
owl:onProperty
n3:RO_0004019
owl:someValuesFrom
n3:SO_0001537
wdrs:describedby
n7:doid.owl