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- NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_assertion type Assertion NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_head.
- 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.
- NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_assertion evidence source_evidence_literature NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_provenance.
- NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_assertion SIO_000772 23415222 NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_provenance.
- NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_assertion wasDerivedFrom befree-20150227 NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_provenance.
- NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_assertion wasGeneratedBy ECO_0000203 NP857886.RA2QnHtK-sB428HTEKNWs1heOY2nfL36-Jag2N04nVkhs130_provenance.