FRINK Linked Data Fragments server

Matches in Wikidata for { <http://www.wikidata.org/entity/Q37539147> ?p ?o ?g. }

• Q37539147 description "article científic" @default.
• Q37539147 description "article scientifique" @default.
• Q37539147 description "articolo scientifico" @default.
• Q37539147 description "artigo científico" @default.
• Q37539147 description "artículu científicu espublizáu en 2013" @default.
• Q37539147 description "bilimsel makale" @default.
• Q37539147 description "scientific article published on 04 December 2013" @default.
• Q37539147 description "vedecký článok" @default.
• Q37539147 description "vetenskaplig artikel" @default.
• Q37539147 description "videnskabelig artikel" @default.
• Q37539147 description "vědecký článek" @default.
• Q37539147 description "wetenschappelijk artikel" @default.
• Q37539147 description "wissenschaftlicher Artikel" @default.
• Q37539147 description "наукова стаття, опублікована в грудні 2013" @default.
• Q37539147 description "научни чланак" @default.
• Q37539147 description "مقالة علمية نشرت في 04 ديسمبر 2013" @default.
• Q37539147 name "Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome" @default.
• Q37539147 name "Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome" @default.
• Q37539147 name "Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome" @default.
• Q37539147 type Item @default.
• Q37539147 label "Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome" @default.
• Q37539147 label "Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome" @default.
• Q37539147 label "Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome" @default.
• Q37539147 prefLabel "Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome" @default.
• Q37539147 prefLabel "Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome" @default.
• Q37539147 prefLabel "Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome" @default.
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