Matches in Wikidata for { <http://www.wikidata.org/entity/Q39762726> ?p ?o ?g. }
- Q39762726 description "2016 nî lūn-bûn" @default.
- Q39762726 description "2016年の論文" @default.
- Q39762726 description "2016年学术文章" @default.
- Q39762726 description "2016年学术文章" @default.
- Q39762726 description "2016年学术文章" @default.
- Q39762726 description "2016年学术文章" @default.
- Q39762726 description "2016年学术文章" @default.
- Q39762726 description "2016年學術文章" @default.
- Q39762726 description "2016年學術文章" @default.
- Q39762726 description "2016年學術文章" @default.
- Q39762726 description "2016年學術文章" @default.
- Q39762726 description "2016年學術文章" @default.
- Q39762726 description "2016年學術文章" @default.
- Q39762726 description "2016년 논문" @default.
- Q39762726 description "article científic" @default.
- Q39762726 description "article scientific" @default.
- Q39762726 description "article scientifique (publié 2016)" @default.
- Q39762726 description "articol științific" @default.
- Q39762726 description "articolo scientifico" @default.
- Q39762726 description "artigo científico (publicado na 2016)" @default.
- Q39762726 description "artigo científico (publicado na 2016)" @default.
- Q39762726 description "artigo científico" @default.
- Q39762726 description "artikull shkencor" @default.
- Q39762726 description "artikulong pang-agham" @default.
- Q39762726 description "artykuł naukowy" @default.
- Q39762726 description "artículo científico publicado en 2016" @default.
- Q39762726 description "artículu científicu espublizáu en 2016" @default.
- Q39762726 description "bilimsel makale" @default.
- Q39762726 description "bài báo khoa học" @default.
- Q39762726 description "mokslinis straipsnis" @default.
- Q39762726 description "naučni članak" @default.
- Q39762726 description "scienca artikolo" @default.
- Q39762726 description "scientific article" @default.
- Q39762726 description "teaduslik artikkel" @default.
- Q39762726 description "tieteellinen artikkeli" @default.
- Q39762726 description "tudományos cikk" @default.
- Q39762726 description "vedecký článok" @default.
- Q39762726 description "vetenskaplig artikel" @default.
- Q39762726 description "videnskabelig artikel (udgivet 2016)" @default.
- Q39762726 description "vitenskapelig artikkel" @default.
- Q39762726 description "vitskapeleg artikkel" @default.
- Q39762726 description "vědecký článek" @default.
- Q39762726 description "wetenschappelijk artikel" @default.
- Q39762726 description "wissenschaftlicher Artikel" @default.
- Q39762726 description "επιστημονικό άρθρο" @default.
- Q39762726 description "мақолаи илмӣ" @default.
- Q39762726 description "мақолаи илмӣ" @default.
- Q39762726 description "наукова стаття, опублікована в травні 2016" @default.
- Q39762726 description "научна статия" @default.
- Q39762726 description "научная статья" @default.
- Q39762726 description "научни чланак" @default.
- Q39762726 description "научни чланак" @default.
- Q39762726 description "գիտական հոդված" @default.
- Q39762726 description "מאמר מדעי" @default.
- Q39762726 description "سائنسی مضمون" @default.
- Q39762726 description "مقالة علمية نشرت بتاريخ 17-5-2016" @default.
- Q39762726 description "مقالهٔ علمی" @default.
- Q39762726 description "২০১৬-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
- Q39762726 description "บทความทางวิทยาศาสตร์" @default.
- Q39762726 description "სამეცნიერო სტატია" @default.
- Q39762726 name "Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy" @default.
- Q39762726 name "Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy" @default.
- Q39762726 type Item @default.
- Q39762726 label "Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy" @default.
- Q39762726 label "Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy" @default.
- Q39762726 prefLabel "Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy" @default.
- Q39762726 prefLabel "Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy" @default.
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