Matches in Wikidata for { <http://www.wikidata.org/entity/Q22008011> ?p ?o ?g. }
- Q22008011 description "1998 nî lūn-bûn" @default.
- Q22008011 description "1998 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած" @default.
- Q22008011 description "1998 թվականի դեկտեմբերին հրատարակված գիտական հոդված" @default.
- Q22008011 description "1998年の論文" @default.
- Q22008011 description "1998年論文" @default.
- Q22008011 description "1998年論文" @default.
- Q22008011 description "1998年論文" @default.
- Q22008011 description "1998年論文" @default.
- Q22008011 description "1998年論文" @default.
- Q22008011 description "1998年论文" @default.
- Q22008011 description "1998年论文" @default.
- Q22008011 description "1998年论文" @default.
- Q22008011 description "1998年论文" @default.
- Q22008011 description "1998年论文" @default.
- Q22008011 description "1998年论文" @default.
- Q22008011 description "1998년 논문" @default.
- Q22008011 description "article científic" @default.
- Q22008011 description "article scientific" @default.
- Q22008011 description "article scientifique (publié 1998-12)" @default.
- Q22008011 description "articol științific" @default.
- Q22008011 description "articolo scientifico (pubblicato il 1998-12)" @default.
- Q22008011 description "artigo científico (publicado na 1998)" @default.
- Q22008011 description "artigo científico (publicado na 1998-12)" @default.
- Q22008011 description "artigo científico" @default.
- Q22008011 description "artikull shkencor" @default.
- Q22008011 description "artikulong pang-agham" @default.
- Q22008011 description "artykuł naukowy" @default.
- Q22008011 description "artículo científico publicado en 1998" @default.
- Q22008011 description "artículu científicu espublizáu en 1998" @default.
- Q22008011 description "bilimsel makale" @default.
- Q22008011 description "bài báo khoa học" @default.
- Q22008011 description "mokslinis straipsnis" @default.
- Q22008011 description "naučni članak" @default.
- Q22008011 description "scienca artikolo" @default.
- Q22008011 description "scientific article" @default.
- Q22008011 description "teaduslik artikkel" @default.
- Q22008011 description "tieteellinen artikkeli" @default.
- Q22008011 description "tudományos cikk" @default.
- Q22008011 description "vedecký článok (publikovaný 1998-12)" @default.
- Q22008011 description "vetenskaplig artikel (publicerad på 1998-12)" @default.
- Q22008011 description "videnskabelig artikel (udgivet 1998-12)" @default.
- Q22008011 description "vitenskapelig artikkel" @default.
- Q22008011 description "vitskapeleg artikkel" @default.
- Q22008011 description "vědecký článek publikovaný v roce 1998" @default.
- Q22008011 description "wetenschappelijk artikel (gepubliceerd op 1998-12)" @default.
- Q22008011 description "wetenskaplike artikel" @default.
- Q22008011 description "wissenschaftlicher Artikel (veröffentlicht in 1998-12)" @default.
- Q22008011 description "επιστημονικό άρθρο" @default.
- Q22008011 description "мақолаи илмӣ" @default.
- Q22008011 description "мақолаи илмӣ" @default.
- Q22008011 description "наукова стаття, опублікована в грудні 1998" @default.
- Q22008011 description "научна статия" @default.
- Q22008011 description "научна статија" @default.
- Q22008011 description "научная статья" @default.
- Q22008011 description "научни чланак (објављен 1998-12)" @default.
- Q22008011 description "научни чланак" @default.
- Q22008011 description "מאמר מדעי" @default.
- Q22008011 description "سائنسی مضمون" @default.
- Q22008011 description "مقالة علمية (نشرت في ديسمبر 1998)" @default.
- Q22008011 description "مقالهٔ علمی" @default.
- Q22008011 description "১৯৯৮-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
- Q22008011 description "ശാസ്ത്ര പ്രബന്ധം" @default.
- Q22008011 description "บทความทางวิทยาศาสตร์" @default.
- Q22008011 description "სამეცნიერო სტატია" @default.
- Q22008011 name "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 name "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 name "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 name "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 type Item @default.
- Q22008011 label "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 label "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 label "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 label "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 prefLabel "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 prefLabel "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 prefLabel "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
- Q22008011 prefLabel "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein" @default.
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