<http://purl.obolibrary.org/obo/DOID_0060486>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:10453"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060486>	<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_0060486>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:178509"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938922	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0060486>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_0060486>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C566822"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060486>	<http://www.w3.org/2000/01/rdf-schema#label>	"Perry syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0060486>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_225> .
<http://purl.obolibrary.org/obo/DOID_0060486>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060486>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060486"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060486>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50938922 .
<http://purl.obolibrary.org/obo/DOID_0060486>	<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_0060486>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:168605"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060486>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A syndrome characterized by parkinsonism, hypoventilation, depression, and weight loss and that has_material_basis_in heterozygous mutation in the DCTN1 gene on chromosome 2p13."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938922	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50938922	<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_0060486>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"parkinsonism with alveolar hypoventilation and mental depression"@en .
<http://purl.obolibrary.org/obo/DOID_0060486>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
_:vb50938922	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .