Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_provenance.
- NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_assertion description "[In all 3 the AGTR1 1166C allele was significantly more common in AAA patients than controls (overall adjusted OR 1.60, 95% CI 1.32 to 1.93, P=1.1x10(-6)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_provenance.
- NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_assertion evidence source_evidence_literature NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_provenance.
- NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_assertion SIO_000772 18239157 NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_provenance.
- NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_assertion wasDerivedFrom befree-20150227 NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_provenance.
- NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_assertion wasGeneratedBy ECO_0000203 NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP229862.RA3Ilr2BqULK_1vX4CTT4E2R-wGKAJ39WnM68N7P3JUG0130_provenance.