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- Q91880082 description "article scientifique publié en 2018" @default.
- Q91880082 description "artículu científicu espublizáu n'agostu de 2018" @default.
- Q91880082 description "scientific article published on 15 August 2018" @default.
- Q91880082 description "wetenschappelijk artikel" @default.
- Q91880082 description "наукова стаття, опублікована в серпні 2018" @default.
- Q91880082 name "High-throughput sequencing reveals distinct genetic features and clinical implications of NSCLC with de novo and acquired EGFR T790M mutation" @default.
- Q91880082 name "High-throughput sequencing reveals distinct genetic features and clinical implications of NSCLC with de novo and acquired EGFR T790M mutation" @default.
- Q91880082 type Item @default.
- Q91880082 label "High-throughput sequencing reveals distinct genetic features and clinical implications of NSCLC with de novo and acquired EGFR T790M mutation" @default.
- Q91880082 label "High-throughput sequencing reveals distinct genetic features and clinical implications of NSCLC with de novo and acquired EGFR T790M mutation" @default.
- Q91880082 prefLabel "High-throughput sequencing reveals distinct genetic features and clinical implications of NSCLC with de novo and acquired EGFR T790M mutation" @default.
- Q91880082 prefLabel "High-throughput sequencing reveals distinct genetic features and clinical implications of NSCLC with de novo and acquired EGFR T790M mutation" @default.
- Q91880082 P1433 Q91880082-66542EB8-E870-4E78-AAF2-0B74A265ABEC @default.
- Q91880082 P1476 Q91880082-A74EB96E-F055-4E85-BEBD-5AF09C0A48F9 @default.
- Q91880082 P2093 Q91880082-0EF8D9DE-AF19-43A9-AC6F-458805F8C965 @default.
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- Q91880082 P2093 Q91880082-5279F8F3-CF98-48C2-9026-368B46191374 @default.
- Q91880082 P2093 Q91880082-5336A292-863B-4A77-87B3-75AD8EEE4989 @default.
- Q91880082 P2093 Q91880082-6DCF3B16-085E-4604-8CE0-CCC470824CD0 @default.
- Q91880082 P2093 Q91880082-90057683-A0C0-45EE-AEA3-349288923095 @default.
- Q91880082 P2093 Q91880082-9262F124-268B-42AB-A9BB-3E5484154ED4 @default.
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- Q91880082 P2093 Q91880082-C8EC9667-6ADA-42C1-B4F4-00E83BF19C69 @default.
- Q91880082 P2093 Q91880082-F8822319-595D-4EA4-8FC1-3BD9003A0F8E @default.
- Q91880082 P304 Q91880082-3672C9BD-45C7-4866-9B3C-2C32FA446BD0 @default.
- Q91880082 P31 Q91880082-D5999DF3-470F-4B87-9165-E10CD67F3576 @default.
- Q91880082 P356 Q91880082-383CA4A8-5BF3-4C5D-A888-87CB1117146E @default.
- Q91880082 P478 Q91880082-FF8C54BA-8AE5-48AD-AD43-54E957E3084C @default.
- Q91880082 P50 Q91880082-C81DEE4D-4091-4568-8349-D6C2FAD9DDD2 @default.
- Q91880082 P577 Q91880082-8CA6DCF5-90E0-4C00-AE8D-DDA0CFA3E7D5 @default.
- Q91880082 P698 Q91880082-5F1D7FC7-B9EC-4267-8995-5553E84537ED @default.
- Q91880082 P921 Q91880082-63D87356-6EC2-4DC3-8DBB-8016D6285E0D @default.
- Q91880082 P921 Q91880082-FD776F25-F737-4007-A722-FCFD533A1EE5 @default.
- Q91880082 P356 J.LUNGCAN.2018.08.014 @default.
- Q91880082 P698 30268462 @default.
- Q91880082 P1433 Q641464 @default.
- Q91880082 P1476 "High-throughput sequencing reveals distinct genetic features and clinical implications of NSCLC with de novo and acquired EGFR T790M mutation" @default.
- Q91880082 P2093 "Han Han-Zhang" @default.
- Q91880082 P2093 "Junyi Ye" @default.
- Q91880082 P2093 "Ke Wang" @default.
- Q91880082 P2093 "Shannon Chuai" @default.
- Q91880082 P2093 "Weimin Li" @default.
- Q91880082 P2093 "Weiya Wang" @default.
- Q91880082 P2093 "Xiaowei Cheng" @default.
- Q91880082 P2093 "Yalun Li" @default.
- Q91880082 P2093 "Ye Wang" @default.
- Q91880082 P2093 "Yuan Tang" @default.
- Q91880082 P304 "205-210" @default.
- Q91880082 P31 Q13442814 @default.
- Q91880082 P356 "10.1016/J.LUNGCAN.2018.08.014" @default.
- Q91880082 P478 "124" @default.
- Q91880082 P50 Q87317866 @default.
- Q91880082 P577 "2018-08-15T00:00:00Z" @default.
- Q91880082 P698 "30268462" @default.
- Q91880082 P921 Q112147935 @default.
- Q91880082 P921 Q3658562 @default.