<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"transmissible spongiform encephalopathy"@en .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A brain disease that is characterized by brain damage resulting from the abnormal folding, clumping and accumulation of cellular proteins in the brain induced by prion proteins."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"KEGG:05020"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_936> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C128346"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Prion protein disease"@en .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0162534"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Prion disease pathway"@en .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Spongiform Encephalopathy"@en .
<http://purl.obolibrary.org/obo/DOID_649>	<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_649>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D017096"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:649"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:A81.9"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"prion induced disorder"@en .
<http://purl.obolibrary.org/obo/DOID_649>	<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_649>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_FlyBase_slim> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.w3.org/2000/01/rdf-schema#label>	"prion disease"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_649>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:20484008"^^<http://www.w3.org/2001/XMLSchema#string> .