This HTML5 document contains 19 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

Prefix	IRI
n5	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	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

n2:DOID_0060333

rdf:type

owl:Class

rdfs:subClassOf

_:vb50938660 n2:DOID_0111143

rdfs:label

mitochondrial complex V (ATP synthase) deficiency nuclear type 4

wdrs:describedby

n5:doid.owl

obo:id

DOID:0060333

obo:created_by

emitraka

obo:creation_date

2015-03-12T16:04:59Z

obo:hasDbXref

ORDO:254913 OMIM:615228 ICD10CM:E88.8

obo:hasExactSynonym

MC5DN4

obo:hasOBONamespace

disease_ontology

obo:inSubset

n8:DO_rare_slim

n2:IAO_0000115

A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the ATP5A1 gene on chromosome 18q.

Subject Item

_:vb50938660

rdf:type

owl:Restriction

owl:onProperty

n2:RO_0004019

owl:someValuesFrom

n2:SO_0001537

wdrs:describedby

n5:doid.owl