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Namespace Prefixes

PrefixIRI
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n2http://purl.obolibrary.org/obo/
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rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
n5http://purl.obolibrary.org/obo/doid#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_678
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_480
rdfs:label
progressive supranuclear palsy
rdfs:comment
Xref MGI. OMIM mapping confirmed by DO. [SN].
wdrs:describedby
n8:doid.owl
obo:id
DOID:678
obo:hasDbXref
NCI:C85028 SNOMEDCT_US_2021_09_01:192975003 OMIM:601104 ORDO:683 MESH:D013494 GARD:7471 UMLS_CUI:C0038868 ICD10CM:G23.1 OMIM:610898 OMIM:609454
obo:hasExactSynonym
Steele-Richardson-Olszewski syndrome progressive supranuclear ophthalmoplegia
obo:hasOBONamespace
disease_ontology
obo:inSubset
n5:DO_rare_slim n5:NCIthesaurus
n2:IAO_0000115
A movement disease that is characterized by serious and progressive problems with control of gait and balance, along with complex eye movement and thinking problems. It involves gradual deterioration and death of specific volumes of the brain.