Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_provenance.
- NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_assertion description "[Combination of the high-risk genotypes (GSTM1 null + GSTT1 null + GSTP1 313 A/G or G/G) demonstrated further increase in the BC risk (OR = 6.64, 95 %CI = 3.63-12.16).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_provenance.
- NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_assertion evidence source_evidence_literature NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_provenance.
- NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_assertion SIO_000772 23054023 NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_provenance.
- NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_assertion wasDerivedFrom befree-2016 NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_provenance.
- NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_assertion wasGeneratedBy ECO_0000203 NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1019785.RAIupWsuiQS77yXJepMIVmZnpkzYYo5o4c6hXViXONgPM130_provenance.