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- source_evidence_literature type ECO_0000212 NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_provenance.
- NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_assertion description "[However, in children an increased risk of ALL (odds ratio [OR] = 1.88; 95% confidence interval [CI], 1.16-3.07; P = .010) and AML (OR = 2.74; 95% CI, 1.07-7.01; P = .036) was observed with the MTR 2756 GG genotype; the association was most pronounced for cases with the MLL translocation (OR = 4.90; 95% CI, 1.30-18.45; P = .019).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_provenance.
- NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_assertion evidence source_evidence_literature NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_provenance.
- NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_assertion SIO_000772 20101025 NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_provenance.
- NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_assertion wasDerivedFrom befree-2016 NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_provenance.
- NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_assertion wasGeneratedBy ECO_0000203 NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_provenance.
- befree-2016 importedOn "2016-02-19" NP789347.RA83HWokOwYDSE4LiaPi0j382T-paLOgW5eLGCzm0dQ9o130_provenance.