<http://purl.obolibrary.org/obo/DOID_0090048>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:10539"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090048>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050837> .
<http://purl.obolibrary.org/obo/DOID_0090048>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:210571"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090048>	<http://www.w3.org/2000/01/rdf-schema#label>	"dystonia 16"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090048>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942159	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0090048>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:612067"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090048>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:G24.1"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090048>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50942159 .
<http://purl.obolibrary.org/obo/DOID_0090048>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50942159	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
_:vb50942159	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50942159	<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_0090048>	<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_0090048>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0090048"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090048>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0090048>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A multifocal dystonia that is characterized by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism, and that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the protein activator of interferon induced protein kinase EIF2AK2 (PRKRA) gene on chromosome 2q31."^^<http://www.w3.org/2001/XMLSchema#string> .