_:vb50941181	<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_0080564>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50941183	<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_0080564>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50941182	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50941182	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SYMP_0000470> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.w3.org/2000/01/rdf-schema#label>	"congenital disorder of glycosylation Il"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:608776"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50941181 .
_:vb50941183	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0004019> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50941182 .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50941183 .
_:vb50941183	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/HP_0001197> .
_:vb50941182	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002452> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:9839"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50941181	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A congenital disorder of glycosylation I that is characterized by progressive microcephaly, hypotonia, developmental delay, drug-resistant infantile epilepsy, and hepatomegaly and has_material_basis_in homozygous mutation in the ALG9 gene on chromosome 11q23."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"congenital disorder of glycosylation 1l"@en .
_:vb50941183	<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_0080564>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:79328"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0080564"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50941181	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50941181	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0080564>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050570> .
_:vb50941182	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .