Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_provenance.
- NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_assertion description "[The SOD2 Val/Val genotype may increase the risk of NSCLC carried by XRCC1 and p53 polymorphisms, particularly for adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_provenance.
- NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_assertion evidence source_evidence_literature NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_provenance.
- NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_assertion SIO_000772 15534883 NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_provenance.
- NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_assertion wasDerivedFrom befree-20140225 NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_provenance.
- NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_assertion wasGeneratedBy ECO_0000203 NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP809552.RASEqPDJIjabw6-bMqGfuQF7Ixt0MRJ1b5TXfopKUji3E130_provenance.