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

PrefixIRI
n6https://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#
n8http://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_0050768
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0111143 _:vb50937554
rdfs:label
mitochondrial complex V (ATP synthase) deficiency, nuclear type 1
wdrs:describedby
n6:doid.owl
obo:id
DOID:0050768
obo:created_by
lschriml
obo:creation_date
2013-02-21T11:26:46Z
obo:hasDbXref
OMIM:604273 ICD10CM:E88.8 ORDO:254913
obo:hasExactSynonym
MC5DN1
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 ATPAF2 gene on chromosome 17p11.
Subject Item
_:vb50937554
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004019
owl:someValuesFrom
n2:SO_0001537
wdrs:describedby
n6:doid.owl