Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_provenance.
- NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_assertion description "[We compared the frequencies of polymorphisms in ten genes that have been hypothesized to have a role in risk of EC (CYP1A1, CYP2A6, CYP2E1, GSTM1, GSTP1, GSTT1, ADH2, ADH3, ALDH2, and O6-MGMT) among three Iranian ethnic groups with highly varying rates of EC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_provenance.
- NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_assertion evidence source_evidence_literature NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_provenance.
- NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_assertion SIO_000772 15327835 NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_provenance.
- NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_assertion wasDerivedFrom gad-20150221 NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_provenance.
- NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_assertion wasGeneratedBy ECO_0000203 NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP50379.RAV8pMCymLEeaxvVctGYeZUH7F7YUHBfRfYvqs2S5_1nk130_provenance.