Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_provenance.
- NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_assertion description "[These results were further supported by the CART analysis which revealed that individuals with the combined genotypes of ESR1-397 CT or TT, ESR1-351 AG or GG and ESR2 -789 AA had the highest risk for GBC [OR = 3.9].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_provenance.
- NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_assertion evidence source_evidence_literature NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_provenance.
- NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_assertion SIO_000772 22808109 NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_provenance.
- NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_assertion wasDerivedFrom befree-20140225 NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_provenance.
- NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_assertion wasGeneratedBy ECO_0000203 NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP183581.RAsK1Zu1B0SSSiD5uakOGEzV3mWMDyR3Sl5027uww2ywU130_provenance.