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- source_evidence_literature type ECO_0000212 NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP914116.RA8h2Zrz3iNCOx7rCTZw72g7_sNiwIx0jNIMrz7zmEyp4130_provenance.