<http://purl.obolibrary.org/obo/DOID_0112079>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112079>	<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_0112079>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"MC1DN24"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50946039	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0112079>	<http://www.w3.org/2000/01/rdf-schema#label>	"nuclear type mitochondrial complex I deficiency 24"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50946039	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
<http://purl.obolibrary.org/obo/DOID_0112079>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0112065> .
_:vb50946039	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0112079>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50946039	<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_0112079>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0112079"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112079>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0112079>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:618245"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112079>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50946039 .
<http://purl.obolibrary.org/obo/DOID_0112079>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFB9 on chromosome 8q24.13."^^<http://www.w3.org/2001/XMLSchema#string> .