@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:Q1101694 rdfs:label "متلازمة جيوبرت"@ar,
        "síndrome de Joubert"@ca,
        "Joubert-Syndrom"@de,
        "Joubert syndrome"@en,
        "sindromo de Joubert"@eo,
        "síndrome de Joubert"@es,
        "Joubertin oireyhtymä"@fi,
        "syndrome de Joubert"@fr,
        "Joubert-szindróma"@hu,
        "sindrome di Joubert"@it,
        "ジュベール症候群"@ja,
        "ჯუბერტის სინდრომი"@ka,
        "주베르 증후군"@ko,
        "Joubert syndroom"@nl,
        "Zespół Joubert"@pl,
        "Síndrome Joubert isolado"@pt,
        "Síndrome Joubert isolado"@pt-br,
        "Joubertov sindrom"@sl,
        "Joubert sendromu"@tr,
        "茹贝尔综合征"@zh,
        "茹贝尔综合征"@zh-cn,
        "茹贝尔综合征"@zh-hans,
        "茹貝爾綜合徵"@zh-hant ;
    schema1:dateModified "2026-10-24T00:22:24+00:00"^^xsd:dateTime ;
    schema1:description "مرض من الأمراض"@ar,
        "trastorn genètic rar"@ca,
        "Krankheit"@de,
        "genetic disorder affecting the cerebellum"@en,
        "rara anomalía de carácter genético"@es,
        "syndrome commençant en période néonatale"@fr,
        "ritka genetikai rendellenesség"@hu,
        "rara malattia genetica che interessa il cervelletto, area del cervello deputata al controllo di equilibrio e coordinazione."@it,
        "rzadki zespół wad genetycznych"@pl,
        "хвороба"@uk ;
    schema1:version 2560165199 ;
    wikibase:identifiers 20,
        22 ;
    wikibase:sitelinks 17 ;
    wikibase:statements 79 ;
    skos:altLabel "síndrome cerebel·looculorenal"@ca,
        "Vermis-Agenesie"@de,
        "CPD IV"@en,
        "Cerebelloparenchymal disorder IV"@en,
        "Classic Joubert syndrome"@en,
        "JBTS"@en,
        "Joubert syndrome type A"@en,
        "Joubert-Boltshauser syndrome"@en,
        "Pure Joubert syndrome"@en,
        "cerebellooculorenal syndrome"@en,
        "Sindrome de Joubert"@es,
        "Joubertin syndrooma"@fi,
        "Agénésie du vermis cérébelleux"@fr,
        "Syndrome cérébello-oculo-rénal"@fr,
        "Syndrome de Joubert-Boltshauser"@fr,
        "Syndrome de joubert"@fr,
        "Agenesia del verme cerebellare"@it,
        "Aplasia del verme cerebellare"@it,
        "Malattia cerebello-parenchimale IV"@it,
        "Sindrome cerebello-oculo-renale"@it,
        "Sindrome di Joubert-Boltshauser"@it,
        "Zespół Jouberta"@pl ;
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    p:P5270 wds:Q1101694-44CE5C4F-B569-4BDD-8C11-AD6885E7F874 ;
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        wds:Q1101694-CB0C9C04-41C1-4A9E-B735-13302995D482 ;
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    p:P665 wds:Q1101694-1098E74C-EFE1-4162-B960-2CBE932E8763 ;
    p:P699 wds:Q1101694-17C97F90-B7AA-4244-A2B6-7F868DCB9E19 ;
    p:P7329 wds:Q1101694-6425E362-1B1A-4F09-997F-60286B2383EB ;
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    p:P7807 wds:Q1101694-6373412F-D185-47F5-9AB0-0BECDF65807C ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0018772> ;
    wdtn:P6366 <https://makg.org/entity/2777386794>,
        <https://makg.org/entity/2911216662> ;
    wdtn:P665 <http://www.kegg.jp/entry/H00530> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050777> ;
    wdt:P10283 "C2777386794" ;
    wdt:P11143 "Joubert syndrome" ;
    wdt:P1325 <http://www.nanbyou.or.jp/entry/4552> ;
    wdt:P138 wd:Q27824559 ;
    wdt:P14914 "D00475" ;
    wdt:P1550 "475" ;
    wdt:P1748 "C74996" ;
    wdt:P1995 wd:Q1071953 ;
    wdt:P2293 wd:Q17145556,
        wd:Q17831998,
        wd:Q18030192,
        wd:Q18030412,
        wd:Q18032971,
        wd:Q18034624,
        wd:Q18034673,
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        wd:Q18035125,
        wd:Q18035406,
        wd:Q18036735,
        wd:Q18037032,
        wd:Q18037090,
        wd:Q18037681,
        wd:Q18038125,
        wd:Q18038587,
        wd:Q18040132,
        wd:Q18040365,
        wd:Q18041269,
        wd:Q18041366,
        wd:Q18042418,
        wd:Q18043134,
        wd:Q18045843,
        wd:Q18045867,
        wd:Q18046183,
        wd:Q18046194,
        wd:Q18046404,
        wd:Q18046421,
        wd:Q18046618,
        wd:Q18046632,
        wd:Q18046646,
        wd:Q18046792,
        wd:Q18048458,
        wd:Q18048834,
        wd:Q18052224,
        wd:Q18053190,
        wd:Q18053376,
        wd:Q18053377,
        wd:Q18054882,
        wd:Q18056094 ;
    wdt:P279 wd:Q15729064,
        wd:Q203031,
        wd:Q55345933 ;
    wdt:P2841 wd:Q21953121 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:0050777>,
        <http://purl.obolibrary.org/obo/DOID_0050777>,
        <http://www.orpha.net/ORDO/Orphanet_475> ;
    wdt:P2892 "C0431399" ;
    wdt:P31 wd:Q112193867,
        wd:Q42303753,
        wd:Q929833 ;
    wdt:P3417 "Joubert-Syndrome" ;
    wdt:P373 "Joubert syndrome" ;
    wdt:P4229 "Q04.3" ;
    wdt:P4233 "jouberts-syndrome" ;
    wdt:P4317 "6802" ;
    wdt:P492 "213300" ;
    wdt:P493 "742.2" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0018772" ;
    wdt:P557 "30688" ;
    wdt:P6366 "2777386794",
        "2911216662" ;
    wdt:P646 "/m/0fm08" ;
    wdt:P6532 wd:Q827017 ;
    wdt:P665 "H00530" ;
    wdt:P699 "DOID:0050777" ;
    wdt:P7329 "LD20.00" ;
    wdt:P7464 "joubert-syndrome" ;
    wdt:P7807 "1414756318" .