<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Griscelli-Prunieras syndrome type 1"@en .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:214450"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060832>	<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_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"GS1"@en .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C1859194"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Griscelli syndrome with neurological impairment"@en .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:2566"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060831> .
<http://purl.obolibrary.org/obo/DOID_0060832>	<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_0060832>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and neurological impairment without immunodeficiency that has_material_basis_in mutations in the MYO5A gene on chromosome 15q21.2."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.w3.org/2000/01/rdf-schema#label>	"Griscelli syndrome type 1"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C537301"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060832"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:79476"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Griscelli syndrome, cutaneous and neurological type"@en .
<http://purl.obolibrary.org/obo/DOID_0060832>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hypopigmentation-neurologic impairment syndrome"@en .