This HTML5 document contains 17 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n7	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3	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#

Statements

Subject Item

n3:DOID_0060351

rdf:type

owl:Class

rdfs:subClassOf

n3:DOID_0111139 _:vb50938690

rdfs:label

mitochondrial complex III deficiency nuclear type 2

wdrs:describedby

n7:doid.owl

obo:id

DOID:0060351

obo:created_by

elvira

obo:creation_date

2015-07-14T16:24:56Z

obo:hasDbXref

OMIM:615157

obo:hasExactSynonym

MC3DN2

obo:hasOBONamespace

disease_ontology

obo:inSubset

n8:DO_FlyBase_slim

n3:IAO_0000115

A mitochondrial metabolism disease characterized by motor disability, with ataxia, apraxia, dystonia, and dysarthria, associated with necrotic lesions throughout the brain and has_material_basis_in mutation in the TTC19 gene on chromosome 17. It has an autosomal recessive inheritance pattern.

Subject Item

_:vb50938690

rdf:type

owl:Restriction

owl:onProperty

n3:RO_0004019

owl:someValuesFrom

n3:SO_0001537

wdrs:describedby

n7:doid.owl