Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_provenance.
- NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_assertion wasGeneratedBy ECO_0000203 NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_provenance.
- NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_assertion wasDerivedFrom befree-20150227 NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_provenance.
- NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_assertion SIO_000772 24413734 NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_provenance.
- NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_assertion evidence source_evidence_literature NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_provenance.
- NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_assertion description "[These analyses identified highly recurrent epigenetic factor mutations in TET2, DNMT3A and IDH2 as well as a new highly prevalent RHOA mutation encoding a p.Gly17Val alteration present in 22 of 35 (67%) angioimmunoblastic T cell lymphoma (AITL) samples and in 8 of 44 (18%) PTCL, not otherwise specified (PTCL-NOS) samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593626.RATMdGtaBXd03xUGgEsooAJ6c5ldRx6C_1IopvUuCdOrQ130_provenance.