@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:Q27677680 rdfs:label "Leber congenital amaurosis 11"@en ;
    schema1:dateModified "2026-07-05T10:59:50+00:00"^^xsd:dateTime ;
    schema1:description "مرض يصيب الإنسان"@ar,
        "Krankheit"@de,
        "Leber congenital amaurosis that has material basis in mutation n the IMPDH1 gene on chromosome 7q31.3-q32"@en,
        "хвороба"@uk ;
    schema1:version 2514100479 ;
    wikibase:identifiers 9 ;
    wikibase:sitelinks 0 ;
    wikibase:statements 18 ;
    skos:altLabel "Amaurosis congenita of Leber, type 11"@en,
        "LCA11"@en,
        "LEBER CONGENITAL AMAUROSIS 11"@en,
        "LEBER CONGENITAL AMAUROSIS 11; LCA11"@en,
        "Leber congenital amaurosis type 11"@en ;
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    wdtn:P486 <http://id.nlm.nih.gov/mesh/C564140> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0013454> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0110216> ;
    wdt:P11430 "DI-03048" ;
    wdt:P2293 wd:Q5972069 ;
    wdt:P279 wd:Q1811132,
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    wdt:P2888 <http://identifiers.org/doid/DOID:0110216>,
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    wdt:P2892 "C1840284" ;
    wdt:P31 wd:Q112193867,
        wd:Q929833 ;
    wdt:P4229 "H35.5" ;
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    wdt:P486 "C564140" ;
    wdt:P492 "146690",
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    wdt:P5270 "MONDO_0013454" ;
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