FRINK Linked Data Fragments server

Matches in Wikidata for { <http://www.wikidata.org/entity/Q94603637> ?p ?o ?g. }

• Q94603637 description "2020 nî lūn-bûn" @default.
• Q94603637 description "2020 թվականի մայիսի 12-ին հրատարակված գիտական հոդված" @default.
• Q94603637 description "2020年の論文" @default.
• Q94603637 description "2020年学术文章" @default.
• Q94603637 description "2020年学术文章" @default.
• Q94603637 description "2020年学术文章" @default.
• Q94603637 description "2020年学术文章" @default.
• Q94603637 description "2020年学术文章" @default.
• Q94603637 description "2020年学术文章" @default.
• Q94603637 description "2020年學術文章" @default.
• Q94603637 description "2020年學術文章" @default.
• Q94603637 description "2020年學術文章" @default.
• Q94603637 description "2020年學術文章" @default.
• Q94603637 description "2020年學術文章" @default.
• Q94603637 description "2020년 논문" @default.
• Q94603637 description "article científic" @default.
• Q94603637 description "article scientific" @default.
• Q94603637 description "article scientifique" @default.
• Q94603637 description "articol științific" @default.
• Q94603637 description "articolo scientifico" @default.
• Q94603637 description "artigo científico" @default.
• Q94603637 description "artigo científico" @default.
• Q94603637 description "artigo científico" @default.
• Q94603637 description "artikel ilmiah" @default.
• Q94603637 description "artikull shkencor" @default.
• Q94603637 description "artikulong pang-agham" @default.
• Q94603637 description "artykuł naukowy" @default.
• Q94603637 description "artículo científico publicado en 2020" @default.
• Q94603637 description "artículu científicu" @default.
• Q94603637 description "bilimsel makale" @default.
• Q94603637 description "bài báo khoa học" @default.
• Q94603637 description "naučni članak" @default.
• Q94603637 description "scienca artikolo" @default.
• Q94603637 description "scientific article published on 12 May 2020" @default.
• Q94603637 description "scientific article published on 12 May 2020" @default.
• Q94603637 description "scientific article published on 12 May 2020" @default.
• Q94603637 description "teaduslik artikkel" @default.
• Q94603637 description "tieteellinen artikkeli" @default.
• Q94603637 description "tudományos cikk" @default.
• Q94603637 description "vedecký článok" @default.
• Q94603637 description "vetenskaplig artikel" @default.
• Q94603637 description "videnskabelig artikel udgivet 12. maj 2020" @default.
• Q94603637 description "vitenskapelig artikkel" @default.
• Q94603637 description "vitskapeleg artikkel" @default.
• Q94603637 description "vědecký článek" @default.
• Q94603637 description "wetenschappelijk artikel" @default.
• Q94603637 description "wissenschaftlicher Artikel" @default.
• Q94603637 description "επιστημονικό άρθρο" @default.
• Q94603637 description "мақолаи илмӣ" @default.
• Q94603637 description "наукова стаття, опублікована в травні 2020" @default.
• Q94603637 description "научна статия" @default.
• Q94603637 description "научная статья" @default.
• Q94603637 description "научни чланак" @default.
• Q94603637 description "научни чланак" @default.
• Q94603637 description "מאמר מדעי" @default.
• Q94603637 description "مقالة علمية نشرت في 12 مايو 2020" @default.
• Q94603637 description "১২ মে ২০২০-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
• Q94603637 description "บทความทางวิทยาศาสตร์" @default.
• Q94603637 description "სამეცნიერო სტატია" @default.
• Q94603637 name "Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM)" @default.
• Q94603637 name "Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM)" @default.
• Q94603637 type Item @default.
• Q94603637 label "Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM)" @default.
• Q94603637 label "Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM)" @default.
• Q94603637 prefLabel "Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM)" @default.
• Q94603637 prefLabel "Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM)" @default.
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