Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_provenance.
- NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_assertion description "[The polymorphic allele, T allele, conferred almost fourfold increased risk of B-NHL (OR = 3.8, 95 %CI = 1.05-13.9), and the risk elevated to be almost eight folds when confined to diffuse large B-cell lymphoma (DLBCL) (OR = 7.9, 95 %CI = 1.67-32.27).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_provenance.
- NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_assertion evidence source_evidence_literature NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_provenance.
- NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_assertion SIO_000772 24627195 NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_provenance.
- NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_assertion wasDerivedFrom befree-2016 NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_provenance.
- NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_assertion wasGeneratedBy ECO_0000203 NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1163722.RApNLJieO-PSXvErrwMfFdmSSKw7IR1HwZhKGg3OIFioc130_provenance.