FRINK Linked Data Fragments server

Matches in Wikidata for { <http://www.wikidata.org/entity/Q51889768> ?p ?o ?g. }

• Q51889768 description "2008 nî lūn-bûn" @default.
• Q51889768 description "2008 թվականի հունիսի 11-ին հրատարակված գիտական հոդված" @default.
• Q51889768 description "2008年の論文" @default.
• Q51889768 description "2008年学术文章" @default.
• Q51889768 description "2008年学术文章" @default.
• Q51889768 description "2008年学术文章" @default.
• Q51889768 description "2008年学术文章" @default.
• Q51889768 description "2008年学术文章" @default.
• Q51889768 description "2008年学术文章" @default.
• Q51889768 description "2008年學術文章" @default.
• Q51889768 description "2008年學術文章" @default.
• Q51889768 description "2008年學術文章" @default.
• Q51889768 description "2008年學術文章" @default.
• Q51889768 description "2008年學術文章" @default.
• Q51889768 description "2008년 논문" @default.
• Q51889768 description "article científic" @default.
• Q51889768 description "article scientific" @default.
• Q51889768 description "article scientifique" @default.
• Q51889768 description "articol științific" @default.
• Q51889768 description "articolo scientifico" @default.
• Q51889768 description "artigo científico" @default.
• Q51889768 description "artigo científico" @default.
• Q51889768 description "artigo científico" @default.
• Q51889768 description "artikel ilmiah" @default.
• Q51889768 description "artikull shkencor" @default.
• Q51889768 description "artikulong pang-agham" @default.
• Q51889768 description "artykuł naukowy" @default.
• Q51889768 description "artículo científico publicado en 2008" @default.
• Q51889768 description "artículu científicu" @default.
• Q51889768 description "bilimsel makale" @default.
• Q51889768 description "bài báo khoa học" @default.
• Q51889768 description "naučni članak" @default.
• Q51889768 description "scienca artikolo" @default.
• Q51889768 description "scientific article published on 11 June 2008" @default.
• Q51889768 description "scientific article published on 11 June 2008" @default.
• Q51889768 description "scientific article published on 11 June 2008" @default.
• Q51889768 description "teaduslik artikkel" @default.
• Q51889768 description "tieteellinen artikkeli" @default.
• Q51889768 description "tudományos cikk" @default.
• Q51889768 description "vedecký článok" @default.
• Q51889768 description "vetenskaplig artikel" @default.
• Q51889768 description "videnskabelig artikel" @default.
• Q51889768 description "vitenskapelig artikkel" @default.
• Q51889768 description "vitskapeleg artikkel" @default.
• Q51889768 description "vědecký článek" @default.
• Q51889768 description "wetenschappelijk artikel" @default.
• Q51889768 description "wissenschaftlicher Artikel" @default.
• Q51889768 description "επιστημονικό άρθρο" @default.
• Q51889768 description "мақолаи илмӣ" @default.
• Q51889768 description "наукова стаття, опублікована в червні 2008" @default.
• Q51889768 description "научна статия" @default.
• Q51889768 description "научная статья" @default.
• Q51889768 description "научни чланак" @default.
• Q51889768 description "научни чланак" @default.
• Q51889768 description "מאמר מדעי" @default.
• Q51889768 description "مقالة علمية نشرت في 11 يونيو 2008" @default.
• Q51889768 description "১১ জুন ২০০৮-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
• Q51889768 description "บทความทางวิทยาศาสตร์" @default.
• Q51889768 description "სამეცნიერო სტატია" @default.
• Q51889768 name "New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome." @default.
• Q51889768 name "New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome." @default.
• Q51889768 type Item @default.
• Q51889768 label "New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome." @default.
• Q51889768 label "New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome." @default.
• Q51889768 prefLabel "New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome." @default.
• Q51889768 prefLabel "New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome." @default.
• Q51889768 P1433 Q51889768-B83B7F4C-1A2C-4A07-B62E-B2C64F4547E8 @default.
• Q51889768 P1476 Q51889768-797A4C3E-78A5-48CD-B340-8931C8431B50 @default.
• Q51889768 P2093 Q51889768-253B2047-7461-4EEA-B06F-88C695E380E0 @default.
• Q51889768 P2093 Q51889768-612A8C3D-8599-48F2-B2F8-C9602CDC72DD @default.
• Q51889768 P2093 Q51889768-7B6B3988-EBAC-49F3-BEA8-7D939FC785F5 @default.
• Q51889768 P2093 Q51889768-89FF0421-38A3-4D32-8AA5-4B4463EA6758 @default.
• Q51889768 P2093 Q51889768-8B95B7C8-6DC2-4481-B6E6-EA2A96F1B715 @default.
• Q51889768 P2093 Q51889768-9AD14934-8210-4E5F-A07B-6CF0C096E7BD @default.
• Q51889768 P2093 Q51889768-D38EB42C-173D-4BE0-A70B-E6F79BF14D32 @default.
• Q51889768 P2093 Q51889768-EA7827D7-167D-4F67-89BD-93FA096EF23B @default.
• Q51889768 P304 Q51889768-F9F0EFA2-E2DE-4C0A-BC6E-608391B1BC02 @default.
• Q51889768 P31 Q51889768-98443C0F-1CDA-448D-9C1B-39C29B78C3CB @default.
• Q51889768 P356 Q51889768-FF69B7CD-66FF-436A-A6BC-4E40CBCB64DF @default.
• Q51889768 P407 Q51889768-AD3DAC07-385B-4713-A495-B4039A3211C8 @default.
• Q51889768 P433 Q51889768-A32DC156-539C-4AB0-B005-1C32F52F97D9 @default.
• Q51889768 P478 Q51889768-28DCE0AF-F186-48D1-98ED-C1ABA8497CAC @default.
• Q51889768 P50 Q51889768-52AC721C-F8FC-4F2C-8244-E42F7FEB2010 @default.
• Q51889768 P50 Q51889768-6404CE4D-32DF-4FB9-ABEA-8F94E6A98679 @default.
• Q51889768 P577 Q51889768-EA44485C-93C8-48EA-8B2B-DC498AFB5499 @default.
• Q51889768 P698 Q51889768-159FF3B9-D1FB-47F9-8805-551D60A914DD @default.
• Q51889768 P356 JMG.2007.056713 @default.
• Q51889768 P698 18550699 @default.
• Q51889768 P1433 Q14640281 @default.
• Q51889768 P1476 "New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome" @default.
• Q51889768 P2093 "A E Pegg" @default.
• Q51889768 P2093 "A L Sertié" @default.
• Q51889768 P2093 "C E Schwartz" @default.
• Q51889768 P2093 "C M C Maranduba" @default.
• Q51889768 P2093 "D E McCloskey" @default.
• Q51889768 P2093 "G de Alencastro" @default.
• Q51889768 P2093 "S E Kliemann" @default.
• Q51889768 P2093 "X Wang" @default.
• Q51889768 P304 "539-543" @default.
• Q51889768 P31 Q13442814 @default.

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