<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:12697"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D000080422"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:G83.5"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0023944"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.w3.org/2000/01/rdf-schema#label>	"locked-in syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:38023001"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_863> .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Locked-in state"@en .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Locked in syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_12697>	<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_12697>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD9CM:344.81"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A nervous system disease that is characterized by complete paralysis of all voluntary muscles except for the ones that control the movements of the eyes."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12697>	<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_12697>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_12697>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:6919"^^<http://www.w3.org/2001/XMLSchema#string> .