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- Q92167521 description "artículu científicu espublizáu n'avientu de 2019" @default.
- Q92167521 description "scientific article published on 21 December 2019" @default.
- Q92167521 description "wetenschappelijk artikel" @default.
- Q92167521 description "наукова стаття, опублікована 21 грудня 2019" @default.
- Q92167521 name "Whole-exome sequencing identifies novel somatic alterations associated with outcomes in idiopathic multicentric Castleman disease" @default.
- Q92167521 name "Whole-exome sequencing identifies novel somatic alterations associated with outcomes in idiopathic multicentric Castleman disease" @default.
- Q92167521 type Item @default.
- Q92167521 label "Whole-exome sequencing identifies novel somatic alterations associated with outcomes in idiopathic multicentric Castleman disease" @default.
- Q92167521 label "Whole-exome sequencing identifies novel somatic alterations associated with outcomes in idiopathic multicentric Castleman disease" @default.
- Q92167521 prefLabel "Whole-exome sequencing identifies novel somatic alterations associated with outcomes in idiopathic multicentric Castleman disease" @default.
- Q92167521 prefLabel "Whole-exome sequencing identifies novel somatic alterations associated with outcomes in idiopathic multicentric Castleman disease" @default.
- Q92167521 P1433 Q92167521-246ED2CD-B154-4FE2-B6C6-1FB1766FCCBE @default.
- Q92167521 P1476 Q92167521-DBB6FF04-FD71-4AB8-A611-1B7917B91455 @default.
- Q92167521 P2093 Q92167521-0865AA6F-F0B5-4856-8476-9A7889E4AC92 @default.
- Q92167521 P2093 Q92167521-376AFACA-1BFB-468D-9F40-1D727F3B673E @default.
- Q92167521 P2093 Q92167521-4A8B2867-E6E0-4F8C-9A62-A8B17A1105DA @default.
- Q92167521 P2093 Q92167521-D6CAE431-3D38-495F-BAAC-42C8B390948F @default.
- Q92167521 P2093 Q92167521-F278EAEE-EDF0-4F81-A849-7B1D0B49C46A @default.
- Q92167521 P304 Q92167521-C410CB7E-BE66-4FBD-8402-EAA5DAD6F4D6 @default.
- Q92167521 P31 Q92167521-3626A51C-F935-44E3-AFC0-57A1FBA971B3 @default.
- Q92167521 P356 Q92167521-EDA81F69-E0E7-4813-90EE-FE25EDE95463 @default.
- Q92167521 P433 Q92167521-166C2981-DD27-4C7E-A263-34D6E880796F @default.
- Q92167521 P478 Q92167521-92B87244-0DC9-429F-92A4-DD391AB2BCAA @default.
- Q92167521 P50 Q92167521-78F41801-13FA-4559-B6E9-CDCBE07EE9CD @default.
- Q92167521 P577 Q92167521-61187DA7-43AF-424A-A2CE-82524A4ACC66 @default.
- Q92167521 P698 Q92167521-5D0A7EEC-FD8E-4FD3-B618-CC58B7BD59A2 @default.
- Q92167521 P921 Q92167521-D67BDE67-C693-44F0-8E7B-A586934B4685 @default.
- Q92167521 P356 BJH.16330 @default.
- Q92167521 P698 31863597 @default.
- Q92167521 P1433 Q4970200 @default.
- Q92167521 P1476 "Whole-exome sequencing identifies novel somatic alterations associated with outcomes in idiopathic multicentric Castleman disease" @default.
- Q92167521 P2093 "Fangjing Shi" @default.
- Q92167521 P2093 "Jing Zhao" @default.
- Q92167521 P2093 "Ken H Young" @default.
- Q92167521 P2093 "Qingqing Lin" @default.
- Q92167521 P2093 "Wenbin Qian" @default.
- Q92167521 P304 "e64-e67" @default.
- Q92167521 P31 Q13442814 @default.
- Q92167521 P356 "10.1111/BJH.16330" @default.
- Q92167521 P433 "5" @default.
- Q92167521 P478 "188" @default.
- Q92167521 P50 Q90030438 @default.
- Q92167521 P577 "2019-12-21T00:00:00Z" @default.
- Q92167521 P698 "31863597" @default.
- Q92167521 P921 Q50349818 @default.