FRINK Linked Data Fragments server

Matches in Wikidata for { <http://www.wikidata.org/entity/Q56331578> ?p ?o ?g. }

• Q56331578 description "2010 nî lūn-bûn" @default.
• Q56331578 description "2010年の論文" @default.
• Q56331578 description "2010年学术文章" @default.
• Q56331578 description "2010年学术文章" @default.
• Q56331578 description "2010年学术文章" @default.
• Q56331578 description "2010年学术文章" @default.
• Q56331578 description "2010年学术文章" @default.
• Q56331578 description "2010年學術文章" @default.
• Q56331578 description "2010年學術文章" @default.
• Q56331578 description "2010年學術文章" @default.
• Q56331578 description "2010年學術文章" @default.
• Q56331578 description "2010年學術文章" @default.
• Q56331578 description "2010年學術文章" @default.
• Q56331578 description "2010년 논문" @default.
• Q56331578 description "article científic" @default.
• Q56331578 description "article scientific" @default.
• Q56331578 description "article scientifique publié en 2010" @default.
• Q56331578 description "articol științific" @default.
• Q56331578 description "articolo scientifico" @default.
• Q56331578 description "artigo científico (publicado na 2010)" @default.
• Q56331578 description "artigo científico (publicado na 2010)" @default.
• Q56331578 description "artigo científico" @default.
• Q56331578 description "artikull shkencor i botuar më 01 shkurt 2010" @default.
• Q56331578 description "artikulong pang-agham" @default.
• Q56331578 description "artykuł naukowy" @default.
• Q56331578 description "artículo científico publicado en 2010" @default.
• Q56331578 description "artículu científicu espublizáu en febreru de 2010" @default.
• Q56331578 description "bilimsel makale" @default.
• Q56331578 description "bài báo khoa học" @default.
• Q56331578 description "im Februar 2010 veröffentlichter wissenschaftlicher Artikel" @default.
• Q56331578 description "mokslinis straipsnis" @default.
• Q56331578 description "naučni članak" @default.
• Q56331578 description "scienca artikolo" @default.
• Q56331578 description "scientific article published on 01 February 2010" @default.
• Q56331578 description "teaduslik artikkel" @default.
• Q56331578 description "tieteellinen artikkeli" @default.
• Q56331578 description "tudományos cikk" @default.
• Q56331578 description "vedecký článok" @default.
• Q56331578 description "vetenskaplig artikel" @default.
• Q56331578 description "videnskabelig artikel (udgivet 2010)" @default.
• Q56331578 description "vitenskapelig artikkel" @default.
• Q56331578 description "vitskapeleg artikkel" @default.
• Q56331578 description "vědecký článek" @default.
• Q56331578 description "wetenschappelijk artikel" @default.
• Q56331578 description "επιστημονικό άρθρο" @default.
• Q56331578 description "мақолаи илмӣ" @default.
• Q56331578 description "мақолаи илмӣ" @default.
• Q56331578 description "наукова стаття, опублікована в лютому 2010" @default.
• Q56331578 description "научна статия" @default.
• Q56331578 description "научная статья" @default.
• Q56331578 description "научни чланак" @default.
• Q56331578 description "научни чланак" @default.
• Q56331578 description "գիտական հոդված" @default.
• Q56331578 description "מאמר מדעי" @default.
• Q56331578 description "سائنسی مضمون" @default.
• Q56331578 description "مقالة علمية" @default.
• Q56331578 description "مقالهٔ علمی" @default.
• Q56331578 description "২০১০-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
• Q56331578 description "บทความทางวิทยาศาสตร์" @default.
• Q56331578 description "სამეცნიერო სტატია" @default.
• Q56331578 name "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1" @default.
• Q56331578 name "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1" @default.
• Q56331578 name "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1" @default.
• Q56331578 type Item @default.
• Q56331578 label "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1" @default.
• Q56331578 label "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1" @default.
• Q56331578 label "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1" @default.
• Q56331578 prefLabel "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1" @default.
• Q56331578 prefLabel "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1" @default.
• Q56331578 prefLabel "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1" @default.
• Q56331578 P1433 Q56331578-A0BC1F03-7B2F-4340-84A4-4EDBFD721DC2 @default.
• Q56331578 P1476 Q56331578-83EBB543-354B-403A-8D0E-E9451F6D44BC @default.
• Q56331578 P2093 Q56331578-98F6677A-BEFC-4A8E-B368-8A7DCD6ED738 @default.
• Q56331578 P2093 Q56331578-C5159DA6-233F-4EB2-B8D6-889E3833D637 @default.
• Q56331578 P304 Q56331578-4223F880-A9EA-49AC-93BE-35267331C303 @default.
• Q56331578 P31 Q56331578-99D32C5F-DEF4-428C-921D-5C0CBA5D6AFA @default.
• Q56331578 P356 Q56331578-0FEF8C62-5770-4D97-8CDB-1EDD0A76598D @default.
• Q56331578 P407 Q56331578-F9DB2F78-2E02-44F0-99F8-00B509AE3AD2 @default.
• Q56331578 P433 Q56331578-7822B945-FA0F-4D41-A5D8-EF2FDE15E008 @default.
• Q56331578 P478 Q56331578-5707B111-A5F5-421C-B919-CD76ECF2E0C3 @default.
• Q56331578 P50 Q56331578-25423E4D-6AC5-40F3-8667-BE90E9735E95 @default.
• Q56331578 P50 Q56331578-E5F31BEC-BBA5-4AB8-A623-BCE72687A6B4 @default.
• Q56331578 P577 Q56331578-4EE618D9-4C10-4179-B8AB-D8DD9F5CD2D6 @default.
• Q56331578 P698 Q56331578-C21E472A-E420-4232-B9EB-1BA1DDFE2645 @default.
• Q56331578 P921 Q56331578-6419F4E5-24F1-4DA2-9BED-5CF2F932079B @default.
• Q56331578 P921 Q56331578-8BB1F6E5-2214-4D3C-9BD9-F4B867318242 @default.
• Q56331578 P921 Q56331578-E84111DE-7729-42EC-980B-FE6EDAF25ABF @default.
• Q56331578 P356 AJMG.A.33234 @default.
• Q56331578 P698 20101680 @default.
• Q56331578 P1433 Q4744254 @default.
• Q56331578 P1476 "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1" @default.
• Q56331578 P2093 "Klaus W Kjaer" @default.
• Q56331578 P2093 "Muhammad Farooq" @default.
• Q56331578 P304 "495-497" @default.
• Q56331578 P31 Q13442814 @default.
• Q56331578 P356 "10.1002/AJMG.A.33234" @default.
• Q56331578 P407 Q1860 @default.
• Q56331578 P433 "2" @default.
• Q56331578 P478 "152A" @default.
• Q56331578 P50 Q30004359 @default.

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