Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_provenance.
- NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_assertion description "[Among 14 870 subjects, the pooled estimated risk of stroke/TIA associated with the 677T allele increased in a dose-dependent manner (T allele pooled OR 1.17, 95%CI 1.09 to 1.26, TT genotype pooled OR 1.37, 95%CI 1.15 to 1.64).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_provenance.
- NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_assertion evidence source_evidence_literature NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_provenance.
- NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_assertion SIO_000772 15947278 NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_provenance.
- NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_assertion wasDerivedFrom befree-20150227 NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_provenance.
- NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_assertion wasGeneratedBy ECO_0000203 NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1001026.RAyP8sHXiu5O_id1CaYDcHzFVkDvgnSDqVu7rhZwoCez0130_provenance.