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- Q82674809 description "article scientifique (publié 2010)" @default.
- Q82674809 description "articolo scientifico (pubblicato il 2010)" @default.
- Q82674809 description "artikull shkencor i botuar më 01 janar 2010" @default.
- Q82674809 description "artículu científicu espublizáu en xineru de 2010" @default.
- Q82674809 description "im Jahr 2010 veröffentlichter wissenschaftlicher Artikel" @default.
- Q82674809 description "scientific article published on 01 January 2010" @default.
- Q82674809 description "wetenschappelijk artikel" @default.
- Q82674809 description "наукова стаття, опублікована в січні 2010" @default.
- Q82674809 name "Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive" @default.
- Q82674809 name "Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive" @default.
- Q82674809 name "Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive" @default.
- Q82674809 type Item @default.
- Q82674809 label "Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive" @default.
- Q82674809 label "Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive" @default.
- Q82674809 label "Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive" @default.
- Q82674809 prefLabel "Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive" @default.
- Q82674809 prefLabel "Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive" @default.
- Q82674809 prefLabel "Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive" @default.
- Q82674809 P1433 Q82674809-6EF718C7-E01E-492A-8146-7D87E64207FA @default.
- Q82674809 P1476 Q82674809-87AC996B-BAE2-4C33-88D0-41E55455EA75 @default.
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- Q82674809 P2093 Q82674809-AEE1CADB-F875-4C2A-B610-72B7B91C4A40 @default.
- Q82674809 P304 Q82674809-DD95A0B5-DC52-4EF1-9DC4-D51491C55E46 @default.
- Q82674809 P31 Q82674809-8BFD3EF3-DF2E-4C39-8450-0752C307F74F @default.
- Q82674809 P433 Q82674809-FB205BB2-50CC-422C-A917-3B5B783A79D8 @default.
- Q82674809 P478 Q82674809-D2FC147E-BC78-4E39-9980-896C513CBDFC @default.
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- Q82674809 P921 Q82674809-6CD7A475-6244-47CD-9D10-C9B3B4BFF411 @default.
- Q82674809 P698 20108392 @default.
- Q82674809 P1433 Q5937167 @default.
- Q82674809 P1476 "Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive" @default.
- Q82674809 P2093 "Fatemeh Alasti" @default.
- Q82674809 P2093 "Guy Van Camp" @default.
- Q82674809 P2093 "Mohammad Hossein Sanati" @default.
- Q82674809 P2093 "Nils Peeters" @default.
- Q82674809 P2093 "Wim Wuyts" @default.
- Q82674809 P304 "116" @default.
- Q82674809 P31 Q13442814 @default.
- Q82674809 P433 "1" @default.
- Q82674809 P478 "127" @default.
- Q82674809 P577 "2010-01-01T00:00:00Z" @default.
- Q82674809 P698 "20108392" @default.
- Q82674809 P921 Q12133 @default.