@prefix p: <http://www.wikidata.org/prop/> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix schema1: <http://schema.org/> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix wd: <http://www.wikidata.org/entity/> .
@prefix wds: <http://www.wikidata.org/entity/statement/> .
@prefix wdt: <http://www.wikidata.org/prop/direct/> .
@prefix wdtn: <http://www.wikidata.org/prop/direct-normalized/> .
@prefix wikibase: <http://wikiba.se/ontology#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

wd:Q21097863 rdfs:label "spinocerebellar ataxia type 15/16"@en ;
    schema1:dateModified "2026-07-05T12:52:49+00:00"^^xsd:dateTime ;
    schema1:description "مرض يصيب الإنسان"@ar,
        "Krankheit"@de,
        "Spinocerebellar ataxia type 15/16 (SCA15/16) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by cerebellar ataxia, tremor and cognitive impairment."@en,
        "хвороба"@uk ;
    schema1:version 2514126475 ;
    wikibase:identifiers 10 ;
    wikibase:sitelinks 0 ;
    wikibase:statements 21 ;
    skos:altLabel "SCA15"@en,
        "SCA15/16"@en,
        "SPINOCEREBELLAR ATAXIA 15"@en,
        "SPINOCEREBELLAR ATAXIA 15; SCA15"@en,
        "Spinocerebellar Ataxia 16"@en,
        "Spinocerebellar Ataxia 16, Formerly"@en,
        "Spinocerebellar Ataxia type 15"@en,
        "spinocerebellar ataxia type 16"@en ;
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    p:P1550 wds:Q21097863-22DC068D-50B5-45CF-AB7F-48779ED56AD3,
        wds:Q21097863-DC49C000-6D94-4B34-9167-0A8586C57F33 ;
    p:P2293 wds:Q21097863-C3AA3CE4-A042-43D9-B0B5-3AD049442D68 ;
    p:P279 wds:Q21097863-1E4FB718-688C-4DB3-A3F5-0D8980F3DB84,
        wds:Q21097863-20EAB4B1-9B2A-428D-916E-F1952C4538BC,
        wds:Q21097863-894EB5D2-EF4B-41F0-8DC6-4A4C9C35D674 ;
    p:P2888 wds:Q21097863-9A8DA436-0659-498C-AE85-7F5103051B5B,
        wds:Q21097863-A43E6600-65FC-42EC-880A-49485FDC8810,
        wds:Q21097863-C6BA2826-F98F-44E3-A3C1-360BF4EB018F,
        wds:Q21097863-E3FE6B21-3BE8-461C-8138-3827957AD412 ;
    p:P2892 wds:Q21097863-378248F0-C3F8-41AE-8501-858430679D4D,
        wds:Q21097863-B5B3C256-8529-4121-A6DE-FC7BB029E63A ;
    p:P31 wds:Q21097863-7220843E-402A-40EC-8019-2411A976DD8C,
        wds:Q21097863-E340512A-5B52-49F9-8D8A-81A10B2B6A23 ;
    p:P4229 wds:Q21097863-AF2D9A7C-6E2F-4618-A062-3162A4BD4B35 ;
    p:P4317 wds:Q21097863-878554DB-94D9-468F-A086-4AECEA93D4DD ;
    p:P492 wds:Q21097863-4BCE9189-182F-457F-925E-D842AE6111D6 ;
    p:P5008 wds:Q21097863-0ACD0745-C9D3-41A5-820B-7BD2EE00AC5E ;
    p:P5270 wds:Q21097863-542E79BA-CE2C-4A20-A775-346C8FA6B8C8 ;
    p:P699 wds:Q21097863-D6C75499-EB0B-48CD-8145-772152622014 ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0011694> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050965> ;
    wdt:P11430 "DI-01078" ;
    wdt:P1550 "98769",
        "98770" ;
    wdt:P2293 wd:Q18028073 ;
    wdt:P279 wd:Q55346087 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:0050965>,
        <http://purl.obolibrary.org/obo/DOID_0050965>,
        <http://www.orpha.net/ORDO/Orphanet_98769>,
        <http://www.orpha.net/ORDO/Orphanet_98770> ;
    wdt:P2892 "C1847725",
        "C2676005" ;
    wdt:P31 wd:Q112193867,
        wd:Q929833 ;
    wdt:P4229 "G11.2" ;
    wdt:P4317 "10477" ;
    wdt:P492 "606658" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0011694" ;
    wdt:P699 "DOID:0050965" .