_:vb50944339	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50944339	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0004019> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.w3.org/2000/01/rdf-schema#label>	"molybdenum cofactor deficiency type B"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:308393"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50944339 .
<http://purl.obolibrary.org/obo/DOID_0111163>	<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_0111163>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C1854989"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"MOCODB"@en .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"molybdenum cofactor deficiency complementation group B"@en .
_:vb50944339	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SO_0001537> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0111165> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:252160"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B"@en .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111163"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50944339	<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_0111163>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:1003368009"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"MOCOD type B"@en .
<http://purl.obolibrary.org/obo/DOID_0111163>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C565373"^^<http://www.w3.org/2001/XMLSchema#string> .