Matches in Wikidata for { <http://www.wikidata.org/entity/Q49922672> ?p ?o ?g. }
- Q49922672 description "2018 nî lūn-bûn" @default.
- Q49922672 description "2018年の論文" @default.
- Q49922672 description "2018年学术文章" @default.
- Q49922672 description "2018年学术文章" @default.
- Q49922672 description "2018年学术文章" @default.
- Q49922672 description "2018年学术文章" @default.
- Q49922672 description "2018年学术文章" @default.
- Q49922672 description "2018年学术文章" @default.
- Q49922672 description "2018年學術文章" @default.
- Q49922672 description "2018年學術文章" @default.
- Q49922672 description "2018年學術文章" @default.
- Q49922672 description "2018年學術文章" @default.
- Q49922672 description "2018年學術文章" @default.
- Q49922672 description "2018년 논문" @default.
- Q49922672 description "article científic" @default.
- Q49922672 description "article scientific" @default.
- Q49922672 description "article scientifique" @default.
- Q49922672 description "articol științific" @default.
- Q49922672 description "articolo scientifico" @default.
- Q49922672 description "artigo científico" @default.
- Q49922672 description "artigo científico" @default.
- Q49922672 description "artigo científico" @default.
- Q49922672 description "artikel ilmiah" @default.
- Q49922672 description "artikull shkencor" @default.
- Q49922672 description "artikulong pang-agham" @default.
- Q49922672 description "artykuł naukowy" @default.
- Q49922672 description "artículo científico publicado en 2018" @default.
- Q49922672 description "artículu científicu" @default.
- Q49922672 description "bilimsel makale" @default.
- Q49922672 description "bài báo khoa học" @default.
- Q49922672 description "naučni članak" @default.
- Q49922672 description "scienca artikolo" @default.
- Q49922672 description "scientific article published on 14 February 2018" @default.
- Q49922672 description "scientific article published on 14 February 2018" @default.
- Q49922672 description "scientific article published on 14 February 2018" @default.
- Q49922672 description "teaduslik artikkel" @default.
- Q49922672 description "tieteellinen artikkeli" @default.
- Q49922672 description "tudományos cikk" @default.
- Q49922672 description "vedecký článok" @default.
- Q49922672 description "vetenskaplig artikel" @default.
- Q49922672 description "videnskabelig artikel" @default.
- Q49922672 description "vitenskapelig artikkel" @default.
- Q49922672 description "vitskapeleg artikkel" @default.
- Q49922672 description "vědecký článek" @default.
- Q49922672 description "wetenschappelijk artikel" @default.
- Q49922672 description "wissenschaftlicher Artikel" @default.
- Q49922672 description "επιστημονικό άρθρο" @default.
- Q49922672 description "мақолаи илмӣ" @default.
- Q49922672 description "наукова стаття, опублікована в лютому 2018" @default.
- Q49922672 description "научна статия" @default.
- Q49922672 description "научная статья" @default.
- Q49922672 description "научни чланак" @default.
- Q49922672 description "научни чланак" @default.
- Q49922672 description "מאמר מדעי" @default.
- Q49922672 description "مقالة علمية نشرت في 14 فبراير 2018" @default.
- Q49922672 description "১৪ ফেব্রুয়ারি ২০১৮-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
- Q49922672 description "บทความทางวิทยาศาสตร์" @default.
- Q49922672 description "სამეცნიერო სტატია" @default.
- Q49922672 name "Variant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular features." @default.
- Q49922672 name "Variant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular features." @default.
- Q49922672 type Item @default.
- Q49922672 label "Variant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular features." @default.
- Q49922672 label "Variant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular features." @default.
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- Q49922672 prefLabel "Variant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular features." @default.
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