@prefix p: <http://www.wikidata.org/prop/> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix schema1: <http://schema.org/> .
@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:Q55787253 rdfs:label "epilepsy and/or ataxia with myoclonus as major feature"@en,
        "Epilepsia e/ou ataxia com mioclonia como característica principal"@pt,
        "Epilepsia e/ou ataxia com mioclonia como característica principal"@pt-br ;
    schema1:dateModified "2026-10-24T00:01:42+00:00"^^xsd:dateTime ;
    schema1:description "human disease"@en,
        "хвороба людини"@uk ;
    schema1:version 2560161470 ;
    wikibase:identifiers 4 ;
    wikibase:sitelinks 0 ;
    wikibase:statements 8 ;
    p:P14914 wds:Q55787253-256CC0AC-7F0F-451D-A2C9-DDFA6902311E ;
    p:P1550 wds:Q55787253-249C8DAA-A6B5-4C71-BD19-1E2B1C43F36D ;
    p:P279 wds:Q55787253-0F353CE7-312C-443C-9957-8B5D091F1B78,
        wds:Q55787253-43E370C1-3382-4889-86CC-A4CA3B78FCF2 ;
    p:P2888 wds:Q55787253-E0E04484-960F-4B74-9319-3F72AE3CFE53 ;
    p:P2892 wds:Q55787253-880858F2-D731-4BD4-AC81-A11B78CDE8FC ;
    p:P31 wds:Q55787253-799F6713-67AA-44B8-99FD-210F16A5247E ;
    p:P5270 wds:Q55787253-208D1EA3-D767-4433-8DC3-36ECEFD9E85F ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0017653> ;
    wdt:P14914 "D306756" ;
    wdt:P1550 "306756" ;
    wdt:P279 wd:Q55787252,
        wd:Q55787264 ;
    wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_306756> ;
    wdt:P2892 "C5681050" ;
    wdt:P31 wd:Q112193867 ;
    wdt:P5270 "MONDO_0017653" .