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- source_evidence_literature type ECO_0000212 NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_provenance.
- NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_assertion description "[None of these tagging SNPs was associated with breast cancer risk, with the exception of XRCC2 rs3218536, R188H, which showed some evidence of a protective association for the rare allele per allele odds ratio, 0.89; 95% confidence intervals (95% CI), 0.80-0.99; P trend = 0.03.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_provenance.
- NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_assertion evidence source_evidence_literature NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_provenance.
- NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_assertion SIO_000772 19064565 NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_provenance.
- NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_assertion wasDerivedFrom gad-20150221 NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_provenance.
- NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_assertion wasGeneratedBy ECO_0000203 NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP135936.RAkgLEJXzWRP1Vov7H8YBzdEi_Eduyy_raPuNnm759jB0130_provenance.