Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_provenance.
- NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_assertion description "[Men homozygous for the C-allele for E185Q (G>C) polymorphism in the NBS1 gene showed an increased BCC risk (OR, 2.19; 95% CI, 1.23-3.91), but not women (OR, 0.84; 95% CI, 0.49-1.47).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_provenance.
- NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_assertion evidence source_evidence_literature NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_provenance.
- NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_assertion SIO_000772 16501254 NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_provenance.
- NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_assertion wasDerivedFrom befree-20140225 NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_provenance.
- NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_assertion wasGeneratedBy ECO_0000203 NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP888859.RAPmAiFoydgb6aRqWRmeGPUMeb3VEpeXEEMSq7Cf_Hpfg130_provenance.