Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_provenance.
- NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_assertion description "[Furthermore, a strong association was observed between the combination of GSTT1 null and GSTM1 null genotype and risk of BC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_provenance.
- NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_assertion evidence source_evidence_literature NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_provenance.
- NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_assertion SIO_000772 22339266 NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_provenance.
- NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_assertion wasDerivedFrom befree-2016 NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_provenance.
- NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_assertion wasGeneratedBy ECO_0000203 NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_provenance.
- befree-2016 importedOn "2016-02-19" NP961233.RA9Uw9PoJMPiFyR_wIENq4Svf3459JEi1dOllUmspy9vU130_provenance.