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- Q93166690 description "article scientifique publié en 2019" @default.
- Q93166690 description "artículu científicu espublizáu en setiembre de 2019" @default.
- Q93166690 description "im September 2019 veröffentlichter wissenschaftlicher Artikel" @default.
- Q93166690 description "scientific article published on 05 September 2019" @default.
- Q93166690 description "wetenschappelijk artikel" @default.
- Q93166690 description "наукова стаття, опублікована 5 вересня 2019" @default.
- Q93166690 name "Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome: Causative variants from pathogenic to likely benign" @default.
- Q93166690 name "Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome: Causative variants from pathogenic to likely benign" @default.
- Q93166690 type Item @default.
- Q93166690 label "Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome: Causative variants from pathogenic to likely benign" @default.
- Q93166690 label "Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome: Causative variants from pathogenic to likely benign" @default.
- Q93166690 prefLabel "Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome: Causative variants from pathogenic to likely benign" @default.
- Q93166690 prefLabel "Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome: Causative variants from pathogenic to likely benign" @default.
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- Q93166690 P1476 Q93166690-3589AF94-A602-41EE-8D48-6610AA43BE04 @default.
- Q93166690 P2093 Q93166690-4937FBB0-1C81-485B-A732-1872C9D937BC @default.
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- Q93166690 P31 Q93166690-8E447115-8DE3-4C2F-AE6C-CFB0C7EB895F @default.
- Q93166690 P356 Q93166690-7FFA9318-F4C6-46EE-BDC4-23C077729312 @default.
- Q93166690 P433 Q93166690-FBD88EA1-8650-4086-92BA-CAA95710593A @default.
- Q93166690 P478 Q93166690-4E6C33C0-9768-47C0-8C60-8A42898F815B @default.
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- Q93166690 P921 Q93166690-1F24E2A5-44C2-4D70-9AC7-10DB70ED6F89 @default.
- Q93166690 P356 J.HRTHM.2019.08.014 @default.
- Q93166690 P698 31493592 @default.
- Q93166690 P1433 Q2058605 @default.
- Q93166690 P1476 "Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome: Causative variants from pathogenic to likely benign" @default.
- Q93166690 P2093 "Connor L Mattivi" @default.
- Q93166690 P2093 "Dan Ye" @default.
- Q93166690 P2093 "Daniel J Clemens" @default.
- Q93166690 P2093 "David J Tester" @default.
- Q93166690 P2093 "John R Giudicessi" @default.
- Q93166690 P2093 "Michael J Ackerman" @default.
- Q93166690 P2093 "Wei Zhou" @default.
- Q93166690 P304 "315-323" @default.
- Q93166690 P31 Q13442814 @default.
- Q93166690 P356 "10.1016/J.HRTHM.2019.08.014" @default.
- Q93166690 P433 "2" @default.
- Q93166690 P478 "17" @default.
- Q93166690 P577 "2019-09-05T00:00:00Z" @default.
- Q93166690 P698 "31493592" @default.
- Q93166690 P921 Q653924 @default.