@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:Q2632848 rdfs:label "شلل نصفي تناوبي في مرحلة الطفولة"@ar,
        "Naizmjenična hemiplegija djetinjstva"@bs,
        "Alternierende Hemiplegie des Kindesalters"@de,
        "alternating hemiplegia of childhood"@en,
        "Hemiplejía alternante de la infancia"@es,
        "Lapsena alkanut vaihteleva toispuolihalvaus"@fi,
        "hémiplégie alternante de l'enfance"@fr,
        "Алтернирачка хемиплегија во детството"@mk,
        "alternating hemiplegia of childhood"@nl,
        "Hemiplegia alternante da infância"@pt,
        "Hemiplegia alternante da infância"@pt-br,
        "Çocukluk çağı alternan hemipleji"@tr ;
    schema1:dateModified "2026-10-23T23:38:41+00:00"^^xsd:dateTime ;
    schema1:description "Krankheit"@de,
        "hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body"@en,
        "trastorno neurológico raro causado por la mutación del gen ATP1A3"@es,
        "maladie rare"@fr,
        "хвороба"@uk ;
    schema1:version 2560156902 ;
    wikibase:identifiers 20 ;
    wikibase:sitelinks 10 ;
    wikibase:statements 40 ;
    skos:altLabel "AHC"@en,
        "AHC1"@en,
        "ALTERNATING HEMIPLEGIA OF CHILDHOOD 1"@en,
        "ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1"@en,
        "Alternating Hemiplegia of Childhood type 1"@en,
        "Hemiplejia alternante de la infancia"@es,
        "Hémiplégie alternante du nourrisson"@fr ;
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    wdtn:P486 <http://id.nlm.nih.gov/mesh/C536589> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0007087> ;
    wdtn:P5806 <http://snomed.info/id/230466004> ;
    wdtn:P6366 <https://makg.org/entity/2777712535> ;
    wdtn:P665 <http://www.kegg.jp/entry/H00998> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050635> ;
    wdt:P11143 "Alternating hemiplegia of childhood" ;
    wdt:P14914 "D02131" ;
    wdt:P1550 "2131" ;
    wdt:P1995 wd:Q83042 ;
    wdt:P2293 wd:Q14904883,
        wd:Q14913170,
        wd:Q15314615,
        wd:Q17832956,
        wd:Q17832965,
        wd:Q17854605,
        wd:Q18029614,
        wd:Q18031394,
        wd:Q18037010 ;
    wdt:P279 wd:Q304497 ;
    wdt:P2841 wd:Q21953125,
        wd:Q21955199 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:0050635>,
        <http://purl.obolibrary.org/obo/DOID_0050635>,
        <http://www.orpha.net/ORDO/Orphanet_2131> ;
    wdt:P2892 "C0338488",
        "C3549447" ;
    wdt:P31 wd:Q112193867,
        wd:Q929833 ;
    wdt:P4229 "G98" ;
    wdt:P4233 "alternating-hemiplegia-of-childhood" ;
    wdt:P4317 "11" ;
    wdt:P486 "C536589" ;
    wdt:P492 "104290",
        "614820" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0007087" ;
    wdt:P557 "33595" ;
    wdt:P5806 "230466004" ;
    wdt:P6366 "2777712535" ;
    wdt:P6532 wd:Q34399420 ;
    wdt:P665 "H00998" ;
    wdt:P668 "NBK1115" ;
    wdt:P673 "1142731" ;
    wdt:P699 "DOID:0050635" ;
    wdt:P7464 "alternating-hemiplegia-of-childhood" .