<http://purl.obolibrary.org/obo/DOID_0060793>	<http://www.w3.org/2000/01/rdf-schema#label>	"hypomyelinating leukodystrophy 5"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060793>	<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_0060793>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060793>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:85163"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060793>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"HLD5"@en .
_:vb50939406	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50939406	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0060793>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hypomyelination-congenital cataract syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0060793>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060793"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50939406	<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_0060793>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:G37.8"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060793>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0060793>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:610532"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060793>	<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_0060793>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50939406 .
_:vb50939406	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0060793>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060786> .
<http://purl.obolibrary.org/obo/DOID_0060793>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A hypomyelinating leukodystrophy characterized by autosomal recessive inheritance of congenital cataract, progressive neurologic impairment, and diffuse myelin deficiency that has_material_basis_in homozygous mutation in the FAM126A gene on chromosome 7p15."^^<http://www.w3.org/2001/XMLSchema#string> .