Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_provenance.
- NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_assertion description "[Because single nucleotide polymorphisms (SNPs) are the most subtle genetic variation in the genome, to examine these hypotheses, we have genotyped 30 SNPs in all five NHEJ genes (Ku70, Ku80, DNA-PKcs, Ligase IV, and XRCC4) in 254 primary breast cancer patients and 379 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_provenance.
- NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_assertion evidence source_evidence_literature NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_provenance.
- NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_assertion SIO_000772 12750264 NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_provenance.
- NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_assertion wasDerivedFrom befree-20140225 NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_provenance.
- NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_assertion wasGeneratedBy ECO_0000203 NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP403271.RAM_QBULKcjQMFGOdUoZNqGr_DGojsyVexTC89oss2pUc130_provenance.