This HTML5 document contains 20 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n7	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
n4	http://purl.obolibrary.org/obo/doid#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_649

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_936

rdfs:label

prion disease

wdrs:describedby

n7:doid.owl

obo:id

DOID:649

obo:hasDbXref

KEGG:05020 NCI:C128346 UMLS_CUI:C0162534 MESH:D017096 ICD10CM:A81.9 SNOMEDCT_US_2021_09_01:20484008

obo:hasExactSynonym

transmissible spongiform encephalopathy Prion protein disease Prion disease pathway Spongiform Encephalopathy prion induced disorder

obo:hasOBONamespace

disease_ontology

obo:inSubset

n4:NCIthesaurus n4:DO_FlyBase_slim

n2: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.