@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:Q749409 rdfs:label "تكون العظم الناقص"@ar,
        "Büllur xəstəliyi"@az,
        "Osteogenesis imperfecta"@bs,
        "osteogènesi imperfecta"@ca,
        "تێکچوونی دروستبوونی ئێسک"@ckb,
        "osteogenesis imperfecta"@cs,
        "Osteogenesis imperfecta"@da,
        "Osteogenesis imperfecta"@de,
        "ατελής οστεογένεση"@el,
        "osteogenesis imperfecta"@en,
        "osteogenesis imperfecta"@en-us,
        "Osteogenesis imperfecta"@eo,
        "osteogénesis imperfecta"@es,
        "osteogenesi inperfektu"@eu,
        "استئوژنز ایمپرفکتا"@fa,
        "osteogenesis imperfecta"@fi,
        "ostéogenèse imparfaite"@fr,
        "siondróm cnámh briosc"@ga,
        "osteoxénese imperfecta"@gl,
        "osteogenesis imperfecta"@gpe,
        "פרכת"@he,
        "आस्टियोजेनेसिस इम्परफेक्टा"@hi,
        "üvegcsontúság"@hu,
        "Անկատար օստեոգենեզ"@hy,
        "Osteogenesis imperfecta"@id,
        "osteogenesi imperfetta"@it,
        "骨形成不全症"@ja,
        "골형성부전증"@ko,
        "Nepilnīgā osteoģenēze"@lv,
        "Остеогенезис имперфекта"@mk,
        "Osteogenesis imperfecta"@ms,
        "osteogenesis imperfecta"@nb,
        "osteogenesis imperfecta"@nl,
        "osteogenesis imperfecta"@nn,
        "ଭଙ୍ଗୁର ଅସ୍ଥି ରୋଗ"@or,
        "wrodzona łamliwość kości"@pl,
        "osteogénese imperfeita"@pt,
        "osteogênese imperfeita"@pt-br,
        "Несовершенный остеогенез"@ru,
        "imperfektna osteogeneza"@sl,
        "osteogenesis imperfecta"@sv,
        "ఆస్టియోజెనిసిస్ ఇంపెర్ఫెక్టా"@te,
        "Osteogenesis İmperfecta"@tr,
        "bệnh xương thủy tinh"@vi,
        "成骨不全症"@zh,
        "成骨不全症"@zh-hans,
        "成骨不全症"@zh-hant,
        "成骨不全症"@zh-hk ;
    schema1:dateModified "2026-10-24T00:30:00+00:00"^^xsd:dateTime ;
    schema1:description "اضطرابات الجينية"@ar,
        "grup de trastorns genètics que provoquen fragilitat òssia"@ca,
        "choroba"@cs,
        "Krankheit"@de,
        "osteochondrodysplasia that has material basis in a deficiency in type-I collagen which results in brittle bones and defective connective tissue"@en,
        "osteochondrodysplasia that has material basis in a deficiency in type-I collagen which results in brittle bones and defective connective tissue"@en-us,
        "trastorno congénito caracterizado por una fragilidad excesiva de las estructuras óseas"@es,
        "hezur-sistemaren garapenaren sortzetiko akatsa"@eu,
        "perinnöllinen sairaus"@fi,
        "groupe de maladies"@fr,
        "doenza conxénita"@gl,
        "group of genetic disorders wey dey result in fragile bones"@gpe,
        "מחלת עצמות"@he,
        "malattia genetica"@it,
        "ମନୁଷ୍ୟଙ୍କ ଏକ ରୋଗ"@or,
        "choroba genetyczna"@pl,
        "doença genética"@pt,
        "osteohondrodisplazija, pri kateri so zaradi pomanjkanja kolagena tipa I kosti krhke in je okvarjeno vezivno tkivo"@sl,
        "genetisk sjukdom"@sv,
        "хвороба"@uk ;
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    wikibase:identifiers 45,
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    wikibase:sitelinks 44 ;
    wikibase:statements 106 ;
    skos:altLabel "malaltia dels ossos de vidre"@ca,
        "síndrome de Lobstein"@ca,
        "fragilitas ossium"@cs,
        "osteopsathyrosis"@cs,
        "Glasknochen"@de,
        "Glasknochenerkrankung"@de,
        "Glasknochenkrankheit"@de,
        "Lobstein's syndrome"@en,
        "OI"@en,
        "Vrolik's disease"@en,
        "brittle bone disease"@en,
        "fragilitas ossium"@en,
        "osteopsathyrosis"@en,
        "osteopsathyrosis idiopathica"@en,
        "huesos de cristal"@es,
        "osteogenesis imperfecta"@es,
        "osteogenia imperfecta"@es,
        "kristalezko hezurren gaixotasun"@eu,
        "OI"@fi,
        "synnynnäinen sidekudossairaus"@fi,
        "hommes de verre"@fr,
        "maladie des os de verre"@fr,
        "osteogenese imparfaite"@fr,
        "ostéogénose imparfaite"@fr,
        "osteoxenia imperfecta"@gl,
        "Ósos de cristal"@gl,
        "Lobstein's syndrome"@gpe,
        "OI"@gpe,
        "Vrolik's disease"@gpe,
        "brittle bone disease"@gpe,
        "fragilitas ossium"@gpe,
        "osteopsathyrosis"@gpe,
        "osteopsathyrosis idiopathica"@gpe,
        "Osteogenesis Imperfecta"@he,
        "אוסטאוגנזה אימפרפקטה"@he,
        "אוסטאוגנזיס אימפרפקטה"@he,
        "אוסטאוגנסיס אימפרפקטה"@he,
        "אוסטיאוגנסיס אימפרפקטה"@he,
        "csontok törékenysége"@hu,
        "osteogenesis imperfecta"@hu,
        "Osteogenesis imperfecta"@it,
        "Penyakit tulang rapuh"@ms,
        "Sindrom Ekman-Lobstein"@ms,
        "Sindrom Vrolik"@ms,
        "fragilitas ossium"@mul,
        "ଓଷ୍ଟିଓଜେନେସିସ ଇମ୍ପରଫେକ୍ଟା"@or,
        "choroba Vrolika"@pl,
        "osteogenesis imperfecta"@pl,
        "samoistna łamliwość kości"@pl,
        "sostnienie niezupełne"@pl,
        "doença de Ekman-Lobstein"@pt,
        "doença de Lobstein"@pt,
        "osso de vidro"@pt,
        "síndrome de Ekman-Lobstein"@pt,
        "síndrome de Lobstein"@pt,
        "Osteogenesis imperfecta"@ru,
        "Врожденная ломкость костей"@ru,
        "Врождённая ломкость костей"@ru,
        "Adair-Dightonov sindrom"@sl,
        "bolezen krhkih kosti"@sl,
        "osteogenesis imperfecta"@sl,
        "osteopsatiroza"@sl,
        "Cam kemik hastalığı"@tr,
        "OI"@tr,
        "先天成骨不全症"@zh,
        "成骨不全"@zh,
        "玻璃娃娃"@zh,
        "玻璃骨"@zh,
        "瓷娃娃"@zh,
        "脆骨"@zh,
        "脆骨病"@zh,
        "脆骨症"@zh ;
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        <http://purl.obolibrary.org/obo/DOID_12347>,
        <http://www.orpha.net/ORDO/Orphanet_666> ;
    wdt:P2892 "C0023931",
        "C0029434" ;
    wdt:P31 wd:Q112193867,
        wd:Q42303753,
        wd:Q929833 ;
    wdt:P3222 "osteogenesis-imperfecta" ;
    wdt:P3417 "Osteogenesis-Imperfecta" ;
    wdt:P3471 "3829" ;
    wdt:P3553 "19828949" ;
    wdt:P373 "Osteogenesis imperfecta" ;
    wdt:P3827 "osteogenesis-imperfecta" ;
    wdt:P4229 "Q78.0" ;
    wdt:P4233 "osteogenesis-imperfecta" ;
    wdt:P4317 "1017" ;
    wdt:P4839 "Entity[\"Disease\", {\"ICDNine756.51\", \"Primary\"}]" ;
    wdt:P486 "D010013" ;
    wdt:P492 "166200" ;
    wdt:P493 "756.51756.51" ;
    wdt:P494 "Q78.078.0" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P508 "21888" ;
    wdt:P557 "866596" ;
    wdt:P604 "001573" ;
    wdt:P6366 "2777668750",
        "2909499170",
        "2909773098" ;
    wdt:P646 "/m/03m7vl" ;
    wdt:P6532 wd:Q18558185 ;
    wdt:P665 "H00506" ;
    wdt:P672 "C05.116.099.708.685",
        "C16.320.737",
        "C17.300.200.540" ;
    wdt:P691 "ph943941" ;
    wdt:P699 "DOID:12347" ;
    wdt:P7329 "LD24.K0" ;
    wdt:P7464 "osteogenesis-imperfecta" ;
    wdt:P7807 "1219932551" ;
    wdt:P8072 "68362" ;
    wdt:P8189 "987007553341805171" ;
    wdt:P9272 "10192" ;
    wdt:P950 "XX553344" .