Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_assertion> ?p ?o ?g. }
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- NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_assertion type Assertion NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_head.
- NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_assertion description "[There was a significant decrease in coronary artery disease incidence in patients carrying a CYP2E1*6 genetic polymorphism (39.7% of the noncarriers vs. 13.6% of the carriers had coronary artery disease; p = 0.019); similar results were found with the haplotype analysis (p = 0.03) but not with CYP2E1*5B alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_provenance.
- NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_assertion evidence source_evidence_literature NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_provenance.
- NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_assertion SIO_000772 20406102 NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_provenance.
- NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_assertion wasDerivedFrom befree-2016 NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_provenance.
- NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_assertion wasGeneratedBy ECO_0000203 NP807115.RAH0luqN3bJcVcMyqDhZpf-vH13-a7lxp3ECC_ijx4Wfs130_provenance.