Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_assertion> ?p ?o ?g. }
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- NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_assertion type Assertion NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_head.
- NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_assertion wasGeneratedBy ECO_0000203 NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_provenance.
- NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_assertion wasDerivedFrom befree-2016 NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_provenance.
- NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_assertion SIO_000772 18807132 NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_provenance.
- NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_assertion evidence source_evidence_literature NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_provenance.
- NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_assertion description "[Multivariate regression analysis showed that cagE, babA2, and IL-1RN-1/2 genotypes were independent predictors of GC, but when patients with benign disorders were grouped together (NUD + DU) and compared with patients with GC, regression analysis disclosed that babA2 (P = 0.000) and IL-1B-31 gene polymorphisms (CC or CT) (P = 0.01) were the only independent markers of GC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694335.RAuocaDKcKn9xGvamBkqo7UruLPNvqDdlHUEMd2oyIeFM130_provenance.