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- Q91509967 description "2019 թվականի հուլիսի 10-ին հրատարակված գիտական հոդված" @default.
- Q91509967 description "artículu científicu espublizáu en xunetu de 2019" @default.
- Q91509967 description "scientific article published on 10 July 2019" @default.
- Q91509967 description "wetenschappelijk artikel" @default.
- Q91509967 description "наукова стаття, опублікована 10 липня 2019" @default.
- Q91509967 name "A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy" @default.
- Q91509967 name "A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy" @default.
- Q91509967 type Item @default.
- Q91509967 label "A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy" @default.
- Q91509967 label "A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy" @default.
- Q91509967 prefLabel "A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy" @default.
- Q91509967 prefLabel "A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy" @default.
- Q91509967 P1433 Q91509967-27D04929-1350-4CE0-9EDE-8341FFD05029 @default.
- Q91509967 P1476 Q91509967-70CD0605-A3DC-4489-847B-3C8E958A68A1 @default.
- Q91509967 P2093 Q91509967-6D734E8A-EADC-4E37-B9F8-2D277964DED0 @default.
- Q91509967 P2093 Q91509967-F6A3B2B6-1A98-418A-9C1B-808284C2589A @default.
- Q91509967 P304 Q91509967-5AC80138-4583-42CA-BD90-5055C6F92AD6 @default.
- Q91509967 P31 Q91509967-4A187A2C-CBAF-4670-AF37-B0937D46F360 @default.
- Q91509967 P356 Q91509967-D813728B-C036-4A78-B284-6B9FD681830B @default.
- Q91509967 P433 Q91509967-10DD7CED-5EF6-40A3-9284-A728E611D45C @default.
- Q91509967 P478 Q91509967-3D83CE52-A841-41D8-812E-973A05663806 @default.
- Q91509967 P50 Q91509967-7A00DE27-1759-4D6E-9C68-E71068CC0E35 @default.
- Q91509967 P50 Q91509967-8BC62368-C123-4C89-BFC5-8DF7C637B922 @default.
- Q91509967 P577 Q91509967-4E9F6F51-7C88-4187-8BD8-52810F06E8A7 @default.
- Q91509967 P698 Q91509967-13944C0C-6982-4A66-A935-9245AEE7931D @default.
- Q91509967 P356 CGE.13596 @default.
- Q91509967 P698 31260566 @default.
- Q91509967 P1433 Q5133760 @default.
- Q91509967 P1476 "A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy" @default.
- Q91509967 P2093 "Dhanya L Narayanan" @default.
- Q91509967 P2093 "Urja Asher" @default.
- Q91509967 P304 "276-277" @default.
- Q91509967 P31 Q13442814 @default.
- Q91509967 P356 "10.1111/CGE.13596" @default.
- Q91509967 P433 "3" @default.
- Q91509967 P478 "96" @default.
- Q91509967 P50 Q54759621 @default.
- Q91509967 P50 Q87699660 @default.
- Q91509967 P577 "2019-07-10T00:00:00Z" @default.
- Q91509967 P698 "31260566" @default.