<http://purl.obolibrary.org/obo/DOID_0080116>	<http://www.w3.org/2000/01/rdf-schema#label>	"mitochondrial complex III deficiency nuclear type 7"@en .
<http://purl.obolibrary.org/obo/DOID_0080116>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080116>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0080116"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50940423	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0004019> .
<http://purl.obolibrary.org/obo/DOID_0080116>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:615824"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50940423	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50940423	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SO_0001537> .
<http://purl.obolibrary.org/obo/DOID_0080116>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0080116>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0111139> .
<http://purl.obolibrary.org/obo/DOID_0080116>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50940423 .
_:vb50940423	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0080116>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_0080116>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC2 gene on chromosome 6p21."^^<http://www.w3.org/2001/XMLSchema#string> .