Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_assertion> ?p ?o ?g. }
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- NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_assertion type Assertion NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_head.
- NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_assertion description "[Significant differences in OS were observed for SM mutated patients grouped based on the presence of combined TET2/DNMT3A/ASXL1 mutations independent of KIT (P = 0.04) and sole TET2 mutations (P<0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_provenance.
- NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_assertion evidence source_evidence_literature NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_provenance.
- NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_assertion SIO_000772 22905207 NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_provenance.
- NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_assertion wasDerivedFrom befree-20150227 NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_provenance.
- NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_assertion wasGeneratedBy ECO_0000203 NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_provenance.