|
rdfs:label
|
"Ataxia espinocerebelar tipo 26"@pt
"Ataxia espinocerebelar tipo 26"@pt-br
"spinocerebellar ataxia type 26"@en
|
|
skos:altLabel
|
"SCA26"@en
|
|
"SPINOCEREBELLAR ATAXIA 26"@en
|
|
"SPINOCEREBELLAR ATAXIA 26; SCA26"@en
|
|
"Spinocerebellar Ataxia type 26"@en
|
|
schema:description
|
"Human disease"@en
"Krankheit"@de
"хвороба людини"@uk
"մարդու հիվանդություն"@hy
"مرض يصيب الإنسان"@ar
|
|
schema:dateModified
|
"2026-10-23T23:18:35+00:00"^^xsd:dateTime
|
|
schema:version
|
2560152234
|
|
wikibase:identifiers
|
10
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
30
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|
p:P11430
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wd:statement/Q21097771-ea35fb9c-4a9a-55f9-d69b-b39cb749dd74
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|
p:P1193
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wd:statement/Q21097771-93EDC024-BC36-4824-9B49-021DCA863B99
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p:P14914
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wd:statement/Q21097771-92AA3735-C53B-4C99-ACB1-99C2CA13906A
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p:P1550
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wd:statement/Q21097771-2CF730C7-F906-455A-9C90-71496A64D6D0
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p:P2293
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wd:statement/Q21097771-87A4BC35-DF1C-4EA7-9927-25FF07E3D9A5
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p:P279
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wd:statement/Q21097771-024B00F7-D6E0-4F87-B057-B19E438C671C
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wd:statement/Q21097771-94C0AB87-26CF-4A37-B312-386B41C2B6C4
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|
wd:statement/Q21097771-F86FFE22-EB59-436F-8968-4F6746C3305E
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|
p:P2841
|
wd:statement/Q21097771-0B1CD70C-09FE-4085-B765-48D6C3DF8A8C
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|
p:P2888
|
wd:statement/Q21097771-2E390E61-C2E3-4C83-A10C-0F0C7EBA09C1
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|
wd:statement/Q21097771-8BA6CBDA-2626-4B4F-BA8E-EB6C22C3DD81
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|
wd:statement/Q21097771-B6E74034-572C-462A-8004-3DC875315DEA
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|
p:P2892
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wd:statement/Q21097771-563A3B7F-F850-453E-86AE-77FA6876588D
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|
p:P31
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wd:statement/Q21097771-42B04BA9-D546-431C-9C69-4C92478226B2
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|
wd:statement/Q21097771-C2F27D6C-CFE8-4D5F-A86F-90CDC0676D86
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|
p:P4229
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wd:statement/Q21097771-1DDEF2E1-2EA8-4445-B9DF-2DB6C74C90CB
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|
p:P4317
|
wd:statement/Q21097771-9A7FA61C-810A-4716-B5C1-0EB9D56F16F2
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|
p:P486
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wd:statement/Q21097771-EE403479-3BEC-4AC6-B961-C510E0E52FE0
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p:P492
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wd:statement/Q21097771-012FE5A5-ADA8-4C46-8002-712A26D0C2D1
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p:P5008
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wd:statement/Q21097771-FB029B82-A453-4655-A342-CE40B9855DAA
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|
p:P5270
|
wd:statement/Q21097771-ECB2B588-8260-45D1-9F17-1271358BD173
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|
p:P6532
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wd:statement/Q21097771-426EE896-BEB8-45A0-AC1E-317BBE07032A
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wd:statement/Q21097771-6EFCE0C4-BEE6-4521-A777-782EB930CA5D
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wd:statement/Q21097771-7F6530F2-4E83-4C92-90EA-8D92FCDA541F
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wd:statement/Q21097771-85779842-A7A9-43EB-AD89-756A3F8F8FCF
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wd:statement/Q21097771-954C8D53-720C-4B0A-9176-761DB24B98F8
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|
wd:statement/Q21097771-AEE97D4E-A173-4032-A787-D4E8169F9E23
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|
wd:statement/Q21097771-B49860D7-67D6-4535-A887-C4611CBC63A9
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wd:statement/Q21097771-E3150554-7474-4C58-89B2-855A8CBB9536
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p:P699
|
wd:statement/Q21097771-908D7135-66E0-4E08-9E7C-C29CD68B7991
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|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C537203>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0012246>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0050975>
|
|
wdt:P11430
|
"DI-03933"
|
|
wdt:P1193
|
0.000001^^xsd:decimal
|
|
wdt:P14914
|
"D101112"
|
|
wdt:P1550
|
"101112"
|
|
wdt:P2293
|
EEF2
|
|
wdt:P279
|
autosomal dominant cerebellar ataxia type III
|
|
wdt:P2841
|
adult onset
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0050975>
|
|
<http://purl.obolibrary.org/obo/DOID_0050975>
|
|
<http://www.orpha.net/ORDO/Orphanet_101112>
|
|
wdt:P2892
|
"C1836395"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"G11.2"
|
|
wdt:P4317
|
"9995"
|
|
wdt:P486
|
"C537203"
|
|
wdt:P492
|
"609306"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0012246"
|
|
wdt:P6532
|
Babinski sign
|
|
Progressive cerebellar ataxia
|
|
Generalized hyperreflexia
|
|
Progressive gait ataxia
|
|
pathologic nystagmus
|
|
dysarthria
|
|
cerebellar atrophy
|
|
truncal ataxia
|
|
wdt:P699
|
"DOID:0050975"
|