Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_assertion> ?p ?o ?g. }
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- NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_assertion type Assertion NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_head.
- 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.
- NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_assertion evidence source_evidence_literature NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_provenance.
- NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_assertion SIO_000772 23415222 NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_provenance.
- NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_assertion wasDerivedFrom befree-2016 NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_provenance.
- NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_assertion wasGeneratedBy ECO_0000203 NP1053466.RAZq2pysPJnhnTg-h4l8bMNsyGgHt_8mNrBtoav31tO4o130_provenance.