Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_provenance.
- NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_assertion description "[The variant allele carriers of XRCC1 (R399Q) polymorphism showed lower risk for recurrence (TaG2; p = 0.05) and death (T2+; p = 0.03) after instillation and radiotherapy than the non-carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_provenance.
- NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_assertion evidence source_evidence_literature NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_provenance.
- NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_assertion SIO_000772 17438703 NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_provenance.
- NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_assertion wasDerivedFrom befree-20140225 NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_provenance.
- NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_assertion wasGeneratedBy ECO_0000203 NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP785724.RAZWup-Ck32Vxd6PzWC_Z2Wd4DxFASMguvKa9z3uJJcVs130_provenance.