@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:Q1436162 rdfs:label "تنكس عصبي مرتبط بكيناز البانتوثينات"@ar,
        "Pantotenat-kinazi pridruženi neurodegeneracijski protein"@bs,
        "neurodegeneració associada a pantotenat-cinasa"@ca,
        "Neurodegeneration mit Eisenablagerung im Gehirn"@de,
        "Νόσος Χάλερβορντεν-Σπατς"@el,
        "pantothenate kinase-associated neurodegeneration"@en,
        "Pantothenate kinase-associated neurodegeneration"@en-ca,
        "Pantothenate kinase-associated neurodegeneration"@en-gb,
        "neurodegeneración asociada a pantotenato quinasa"@es,
        "PKAN-tauti"@fi,
        "neurodégénerescence associée à la pantothénate kinase"@fr,
        "PKAN"@id,
        "sindrome di Hallervorden-Spatz"@it,
        "パントテン酸キナーゼ関連神経変性症"@ja,
        "Pantotenate kinase-assosiert nevrodegenerativ sykdom"@nb,
        "syndroom van Hallervorden-Spatz"@nl,
        "Choroba Hallervordena-Spatza"@pl,
        "neurodegeneração associada a pantotenato quinase"@pt,
        "Neurodegeneração associada a pantotenato quinase"@pt-br,
        "Болезнь Галлервордена—Шпатца"@ru,
        "泛酸鹽激活酵素關聯之神經退化性疾病"@zh,
        "泛酸鹽激活酵素關聯之神經退化性疾病"@zh-hans,
        "泛酸鹽啟用酵素關聯之神經退化性疾病"@zh-hant ;
    schema1:dateModified "2026-10-23T23:26:58+00:00"^^xsd:dateTime ;
    schema1:description "Krankheit"@de,
        "neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13"@en,
        "dégénérescence cérébrale par accumulation de fer dans les noyaux gris centraux"@fr,
        "malattia autosomica recessiva, legata al cromosoma 20,caratterizzata da degenerazione cerebrale"@it,
        "Doença genética neurodegenerativa com acumulação de ferro no cérebro"@pt,
        "хвороба"@uk ;
    schema1:version 2560154744 ;
    wikibase:identifiers 27,
        30 ;
    wikibase:sitelinks 18 ;
    wikibase:statements 50 ;
    skos:altLabel "νευροεκφυλισμός που σχετίζεται με την παντοθενική κινάση"@el,
        "Hallervorden-Spatz disease"@en,
        "Hallervorden-Spatz syndrome"@en,
        "NBIA1"@en,
        "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1"@en,
        "Neurodegeneration With Brain Iron Accumulation type 1"@en,
        "PKAN"@en,
        "Pantothenate Kinase-Associated Neurodegeneration"@en,
        "Pigmentary pallidal degeneration"@en,
        "Pkan Neuroaxonal Dystrophy, Juvenile-Onset"@en,
        "brain Iron Accumulation type I syndrome"@en,
        "neurodegeneration with brain iron accumulation 1"@en,
        "pigmentary pallidal degeneration (disorder)"@en,
        "Neurodegeneracion asociada a pantotenato quinasa"@es,
        "neurodegenerazione con accumulo di ferro"@it,
        "neurodegenerazione con accumulo di ferro a livello cerebrale"@it ;
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