|
rdfs:label
|
"Ataxia espinocerebelar tipo 23"@pt
"Ataxia espinocerebelar tipo 23"@pt-br
"spinocerebellar ataxia type 23"@en
|
|
skos:altLabel
|
"SCA23"@en
|
|
"SPINOCEREBELLAR ATAXIA 23"@en
|
|
"SPINOCEREBELLAR ATAXIA 23; SCA23"@en
|
|
"Spinocerebellar Ataxia type 23"@en
|
|
schema:description
|
"Human disease"@en
"Krankheit"@de
"хвороба людини"@uk
"مرض يصيب الإنسان"@ar
|
|
schema:dateModified
|
"2026-10-23T23:18:33+00:00"^^xsd:dateTime
|
|
schema:version
|
2560152224
|
|
wikibase:identifiers
|
10
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
27
|
|
p:P11430
|
wd:statement/Q21097865-a13790c5-4242-1475-5973-5e726cba8e77
|
|
p:P1193
|
wd:statement/Q21097865-B1246C0B-2A1D-4182-BE0B-95029D67AB11
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|
p:P14914
|
wd:statement/Q21097865-18882004-B107-4C81-9033-9CE8B70F0605
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|
p:P1550
|
wd:statement/Q21097865-3B643AE5-B25B-4F34-B67B-4B6FF1CC3AC2
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|
p:P2293
|
wd:statement/Q21097865-98F8505A-2BDF-46D2-9860-426C08DA4B05
|
|
p:P279
|
wd:statement/Q21097865-46E10960-9A56-4C67-A4A5-5BB382C59F83
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|
wd:statement/Q21097865-A2DE3E1E-A31B-4B5E-A922-A174E7C24A64
|
|
wd:statement/Q21097865-CA395289-10B6-412B-AA80-A27C62D0D387
|
|
p:P2841
|
wd:statement/Q21097865-9CCB18E9-ECE4-4A36-BB19-3EA45BB65884
|
|
p:P2888
|
wd:statement/Q21097865-1A18BFCE-3051-4FA7-AA1B-183AFF15672F
|
|
wd:statement/Q21097865-8DD1D84B-9390-4DF9-96E1-5F46063ED7DB
|
|
wd:statement/Q21097865-E26BCA8E-EE89-4A5A-9A80-8D0699C8DCC2
|
|
p:P2892
|
wd:statement/Q21097865-B6E409E3-96EF-4788-AD49-99EADDC29D80
|
|
p:P31
|
wd:statement/Q21097865-BAA84C68-1ACB-4340-9A3D-7D15342EA27E
|
|
wd:statement/Q21097865-D73C1ADB-EFFC-4E62-B660-5799AB0F926D
|
|
p:P4229
|
wd:statement/Q21097865-D4483037-67B9-4A96-9D43-56B090FBE494
|
|
p:P4317
|
wd:statement/Q21097865-28EB78A3-AD54-455E-8888-913A786961DA
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|
p:P486
|
wd:statement/Q21097865-86EA5966-AC8D-4535-9653-243403B9E2FA
|
|
p:P492
|
wd:statement/Q21097865-9A2AF2AE-939F-45CA-9384-34E2EB319004
|
|
p:P5008
|
wd:statement/Q21097865-F56FF956-521D-4770-8069-6F0AF9476C65
|
|
p:P5270
|
wd:statement/Q21097865-F3C1A18D-4667-4E72-AF8F-B3DE1D0AFBFD
|
|
p:P6532
|
wd:statement/Q21097865-2247E320-3214-4F30-A665-E6BE1F401305
|
|
wd:statement/Q21097865-2884AAF3-F2DE-4FFE-94A7-CD6BE5181972
|
|
wd:statement/Q21097865-2E3BE0E8-B6A5-46A9-87B4-0A160B6AFF2F
|
|
wd:statement/Q21097865-73B9F87C-D0D8-49E2-A67B-646E21EB7DC7
|
|
wd:statement/Q21097865-C920C9C3-1BF3-4447-A22F-C6754B5FEC50
|
|
p:P699
|
wd:statement/Q21097865-39C36DCE-3CE7-4B5B-8799-DCBAA8CE05F1
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C537201>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0012449>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0050973>
|
|
wdt:P11430
|
"DI-02949"
|
|
wdt:P1193
|
0.000001^^xsd:decimal
|
|
wdt:P14914
|
"D101108"
|
|
wdt:P1550
|
"101108"
|
|
wdt:P2293
|
PDYN
|
|
wdt:P279
|
autosomal dominant cerebellar ataxia type I
|
|
wdt:P2841
|
adult onset
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0050973>
|
|
<http://purl.obolibrary.org/obo/DOID_0050973>
|
|
<http://www.orpha.net/ORDO/Orphanet_101108>
|
|
wdt:P2892
|
"C1853250"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"G11.2"
|
|
wdt:P4317
|
"9950"
|
|
wdt:P486
|
"C537201"
|
|
wdt:P492
|
"610245"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0012449"
|
|
wdt:P6532
|
agenesis of the corpus callosum
|
|
Progressive cerebellar ataxia
|
|
cerebellar atrophy
|
|
impaired proprioception
|
|
dysmetria
|
|
wdt:P699
|
"DOID:0050973"
|