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- source_evidence_literature type ECO_0000212 NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_provenance.
- NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_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." NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_provenance.
- NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_assertion evidence source_evidence_literature NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_provenance.
- NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_assertion SIO_000772 20101025 NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_provenance.
- NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_assertion wasDerivedFrom gad-20150221 NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_provenance.
- NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_assertion wasGeneratedBy ECO_0000203 NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP129893.RASRZ1Znl9Kbikm6Z2xJj0SLryYk5bYtCHL_l9im_1kr4130_provenance.