Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP205871.RAug5LcgY_uhsVKfd-7AOq47sDTzMOxCIotKx0lmzcdN4130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205871.RAug5LcgY_uhsVKfd-7AOq47sDTzMOxCIotKx0lmzcdN4130_provenance.
• NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197539.RAzFfhx_spOXT3bCl_cc9EUfcvmAPvkmfTIezXoYNkPY0130_provenance.
• NP640361.RA2xVCqTVGGlbPRYkikPMmMbBm7IHz3bLjkj-VY2NnkGQ130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640361.RA2xVCqTVGGlbPRYkikPMmMbBm7IHz3bLjkj-VY2NnkGQ130_provenance.
• NP742226.RA--S2Q5AKuYW4xystLcBRSXOTjuj7OAZ_t2V7QTbuKkE130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742226.RA--S2Q5AKuYW4xystLcBRSXOTjuj7OAZ_t2V7QTbuKkE130_provenance.
• assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_provenance.
• NP873128.RAnO8fOoKGOc_xuMq36lDH4r8OXStQ8CyAiXXrxT6P1is130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873128.RAnO8fOoKGOc_xuMq36lDH4r8OXStQ8CyAiXXrxT6P1is130_provenance.
• NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1053468.RAv4yJecE7X3tFXdKPLXNWXzTfQaU7Ezo3RJuPzHoxrYg130_provenance.
• NP582904.RAN31ExyytSIr-wz1SRmjJzfSahuwRLlFICLYYoQN7mao130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582904.RAN31ExyytSIr-wz1SRmjJzfSahuwRLlFICLYYoQN7mao130_provenance.
• NP1053465.RAMkAWxsXBAlTkOJzozxiwRrPwl4aw_pPe6LF2FHvuLU0130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1053465.RAMkAWxsXBAlTkOJzozxiwRrPwl4aw_pPe6LF2FHvuLU0130_provenance.
• NP1053467.RAPEr912S_uOUBpH2O37C_af5PZqppiBc7Jel8BYQ4XSE130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1053467.RAPEr912S_uOUBpH2O37C_af5PZqppiBc7Jel8BYQ4XSE130_provenance.
• NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_assertion description "[We identified driver mutations as predominantly clonal (e.g., MYD88, trisomy 12, and del(13q)) or subclonal (e.g., SF3B1 and TP53), corresponding to earlier and later events in CLL evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_provenance.