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- source_evidence_literature type ECO_0000212 NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_provenance.
- NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_assertion description "[We further showed that inferior OS and DSS were most pronounced in patients whose lymphomas contained both TNFRSF14 mutations and 1p36 deletions after adjustment for the International Prognostic Index [hazard ratios of 3.65 (95% confidence interval, 1.35-9.878, P=0.011) and 3.19 (95% confidence interval, 1.06-9.57, P=0.039), respectively].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_provenance.
- NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_assertion evidence source_evidence_literature NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_provenance.
- NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_assertion SIO_000772 20884631 NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_provenance.
- NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_assertion wasDerivedFrom befree-20150227 NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_provenance.
- NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_assertion wasGeneratedBy ECO_0000203 NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP804742.RAP-uhMo3uHkIbCcelcjdK4cT9NHYyqqm3n96dXngOUPg130_provenance.