FRINK Linked Data Fragments server

Matches in Wikidata for { <http://www.wikidata.org/entity/Q37002477> ?p ?o ?g. }

• Q37002477 description "article científic" @default.
• Q37002477 description "article scientifique" @default.
• Q37002477 description "articolo scientifico" @default.
• Q37002477 description "artigo científico" @default.
• Q37002477 description "artículu científicu espublizáu en 2008" @default.
• Q37002477 description "bilimsel makale" @default.
• Q37002477 description "scientific article published on September 2008" @default.
• Q37002477 description "vedecký článok" @default.
• Q37002477 description "vetenskaplig artikel" @default.
• Q37002477 description "videnskabelig artikel" @default.
• Q37002477 description "vědecký článek" @default.
• Q37002477 description "wetenschappelijk artikel" @default.
• Q37002477 description "wissenschaftlicher Artikel" @default.
• Q37002477 description "наукова стаття, опублікована у вересні 2008" @default.
• Q37002477 description "научни чланак" @default.
• Q37002477 description "مقالة علمية نشرت في سبتمبر 2008" @default.
• Q37002477 name "A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction" @default.
• Q37002477 name "A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction" @default.
• Q37002477 name "A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction." @default.
• Q37002477 type Item @default.
• Q37002477 label "A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction" @default.
• Q37002477 label "A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction" @default.
• Q37002477 label "A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction." @default.
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• Q37002477 prefLabel "A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction." @default.
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• Q37002477 P1476 "A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction" @default.
• Q37002477 P2093 "Catherine P Lu" @default.
• Q37002477 P2093 "David B Roth" @default.
• Q37002477 P2093 "Serre-Yu Wong" @default.
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