About: prion disease

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	brain disease
label	prion disease
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:649
database_cross_reference	ICD10CM:A81.9 KEGG:05020 MESH:D017096 NCI:C128346 SNOMEDCT_US_2021_09_01:20484008 UMLS_CUI:C0162534
has_exact_synonym	Prion disease pathway (en) Prion protein disease (en) Spongiform Encephalopathy (en) prion induced disorder (en) transmissible spongiform encephalopathy (en)
has_obo_namespace	disease_ontology
in_subset	DO_FlyBase_slim NCIthesaurus
http://purl.obolib...g/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.
is subClassOf of	Creutzfeldt-Jakob disease chronic wasting disease Gerstmann-Straussler-Scheinker syndrome scrapie variant Creutzfeldt-Jakob disease kuru fatal familial insomnia Huntington's disease-like 1
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50954792

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