FRINK Linked Data Fragments server

Matches in Wikidata for { <http://www.wikidata.org/entity/Q49052576> ?p ?o ?g. }

• Q49052576 description "2014 nî lūn-bûn" @default.
• Q49052576 description "2014年の論文" @default.
• Q49052576 description "2014年学术文章" @default.
• Q49052576 description "2014年学术文章" @default.
• Q49052576 description "2014年学术文章" @default.
• Q49052576 description "2014年学术文章" @default.
• Q49052576 description "2014年学术文章" @default.
• Q49052576 description "2014年学术文章" @default.
• Q49052576 description "2014年學術文章" @default.
• Q49052576 description "2014年學術文章" @default.
• Q49052576 description "2014年學術文章" @default.
• Q49052576 description "2014年學術文章" @default.
• Q49052576 description "2014年學術文章" @default.
• Q49052576 description "2014년 논문" @default.
• Q49052576 description "article científic" @default.
• Q49052576 description "article scientific" @default.
• Q49052576 description "article scientifique" @default.
• Q49052576 description "articol științific" @default.
• Q49052576 description "articolo scientifico" @default.
• Q49052576 description "artigo científico" @default.
• Q49052576 description "artigo científico" @default.
• Q49052576 description "artigo científico" @default.
• Q49052576 description "artikel ilmiah" @default.
• Q49052576 description "artikull shkencor" @default.
• Q49052576 description "artikulong pang-agham" @default.
• Q49052576 description "artykuł naukowy" @default.
• Q49052576 description "artículo científico publicado en 2014" @default.
• Q49052576 description "artículu científicu" @default.
• Q49052576 description "bilimsel makale" @default.
• Q49052576 description "bài báo khoa học" @default.
• Q49052576 description "naučni članak" @default.
• Q49052576 description "scienca artikolo" @default.
• Q49052576 description "scientific article published on 14 August 2014" @default.
• Q49052576 description "scientific article published on 14 August 2014" @default.
• Q49052576 description "scientific article published on 14 August 2014" @default.
• Q49052576 description "teaduslik artikkel" @default.
• Q49052576 description "tieteellinen artikkeli" @default.
• Q49052576 description "tudományos cikk" @default.
• Q49052576 description "vedecký článok" @default.
• Q49052576 description "vetenskaplig artikel" @default.
• Q49052576 description "videnskabelig artikel" @default.
• Q49052576 description "vitenskapelig artikkel" @default.
• Q49052576 description "vitskapeleg artikkel" @default.
• Q49052576 description "vědecký článek" @default.
• Q49052576 description "wetenschappelijk artikel" @default.
• Q49052576 description "wissenschaftlicher Artikel" @default.
• Q49052576 description "επιστημονικό άρθρο" @default.
• Q49052576 description "мақолаи илмӣ" @default.
• Q49052576 description "наукова стаття, опублікована в серпні 2014" @default.
• Q49052576 description "научна статия" @default.
• Q49052576 description "научная статья" @default.
• Q49052576 description "научни чланак" @default.
• Q49052576 description "научни чланак" @default.
• Q49052576 description "מאמר מדעי" @default.
• Q49052576 description "مقالة علمية نشرت في 14 أغسطس 2014" @default.
• Q49052576 description "১৪ আগস্ট ২০১৪-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
• Q49052576 description "บทความทางวิทยาศาสตร์" @default.
• Q49052576 description "სამეცნიერო სტატია" @default.
• Q49052576 name "Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion." @default.
• Q49052576 name "Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion." @default.
• Q49052576 type Item @default.
• Q49052576 label "Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion." @default.
• Q49052576 label "Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion." @default.
• Q49052576 prefLabel "Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion." @default.
• Q49052576 prefLabel "Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion." @default.
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