Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_assertion type Assertion NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_head.
- NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_assertion description "[Analysis of the possible interactions between the genotypes, after adjustment for the risk factors, demonstrated that individuals carrying CYP1A1 variant GSTT1 null genotypes had an 8.907-fold increased CAD risk compared to their wild status (p<0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_provenance.
- NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_assertion evidence source_evidence_literature NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_provenance.
- NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_assertion SIO_000772 21848428 NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_provenance.
- NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_assertion wasDerivedFrom befree-20140225 NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_provenance.
- NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_assertion wasGeneratedBy ECO_0000203 NP576876.RAAxnJotaDhf6rY2f-ngVO5IBereBTkORPYl3RBzpYvfg130_provenance.