@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:Q147270 rdfs:label "حثل المخروطية"@ar,
        "Distròfia de Cons i Bastons"@ca,
        "Zapfen-Stäbchen-Dystrophie"@de,
        "cone dystrophy"@en,
        "cone dystrophy"@en-ca,
        "cone dystrophy"@en-gb,
        "Distrofia de conos y bastones"@es,
        "dystrophie des cônes"@fr,
        "דיסטרופיה של המדוכים"@he,
        "Distrofia di coni e bastoncelli"@it,
        "錐体ジストロフィー"@ja,
        "Дистрофия колбочек"@ru,
        "distrofija čepnic"@sl,
        "Tappdystrofi"@sv,
        "Көчәюче колбачыклы дистрофия"@tt ;
    schema1:dateModified "2026-10-23T03:53:52+00:00"^^xsd:dateTime ;
    schema1:description "malaltia hereditària que afecta a l'ull i provoca pèrdua de visió"@ca,
        "Krankheit"@de,
        "inherited ocular disorder characterized by the loss of cone cells"@en,
        "inherited ocular disorder characterized by the loss of cone cells"@en-ca,
        "inherited ocular disorder characterized by the loss of cone cells"@en-gb,
        "maladie de l'oeuil"@fr,
        "Глазное расстройство по причине наследственности"@ru,
        "хвороба"@uk ;
    schema1:version 2559838805 ;
    wikibase:identifiers 19 ;
    wikibase:sitelinks 10 ;
    wikibase:statements 33 ;
    skos:altLabel "Cone Dystrophy, Autosomal Dominant"@en,
        "RCD1"@en,
        "RETINAL CONE DYSTROPHY 1"@en,
        "RETINAL CONE DYSTROPHY 1; RCD1"@en,
        "Retinal Cone Degeneration"@en,
        "retinal cone dystrophy"@en,
        "Distrofia de conos"@es ;
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    p:P18 wds:Q147270-d64552f6-4d02-fd23-8b27-52224ec6defc ;
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        wds:Q147270-9DE15711-A77E-44C9-87B5-E8F314FEAF06,
        wds:Q147270-D404D975-951B-4F82-B27B-D2D28712F6CF,
        wds:Q147270-D9EC24E7-522E-437E-8E64-6BEAB7586AEA ;
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    p:P699 wds:Q147270-55E88A87-445C-465F-99AD-70213F374A3D ;
    wdtn:P2581 <http://babelnet.org/rdf/s01749600n> ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/D000077765> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0008374> ;
    wdtn:P6366 <https://makg.org/entity/2778758327> ;
    wdtn:P672 <http://id.nlm.nih.gov/mesh/C11.270.151>,
        <http://id.nlm.nih.gov/mesh/C11.768.216> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050795> ;
    wdt:P11143 "Cone dystrophy" ;
    wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/Fundus%20of%20a%20patient%20with%20cone%20rod%20dystrophy.png> ;
    wdt:P1995 wd:Q161437 ;
    wdt:P2293 wd:Q18030411,
        wd:Q18030414,
        wd:Q18048723,
        wd:Q18052862 ;
    wdt:P2581 "01749600n" ;
    wdt:P279 wd:Q550455 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:0050795>,
        <http://purl.obolibrary.org/obo/DOID_0050795>,
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    wdt:P2892 "C0730290",
        "C1867326" ;
    wdt:P31 wd:Q112193867,
        wd:Q929833 ;
    wdt:P373 "Cone dystrophy" ;
    wdt:P3841 "HP:0008020" ;
    wdt:P4233 "cone-dystrophy" ;
    wdt:P4317 "10790" ;
    wdt:P486 "D000077765" ;
    wdt:P492 "180020",
        "610024",
        "610356",
        "610478",
        "613093" ;
    wdt:P494 "H35.5" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0008374" ;
    wdt:P6366 "2778758327" ;
    wdt:P672 "C11.270.151",
        "C11.768.216" ;
    wdt:P699 "DOID:0050795" .