Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_assertion type Assertion NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_head.
- NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_assertion description "[MG 18?2 showed an enrichment (P-value?=?0.002) of significant associations with CHD-associated SNPs (P-value?=?1.2�10-7 for association with rs964184 in the ZNF259/APOA5 region) and a weak, but positive causal effect (odds ratio?=?1.05 per SD increment in MG 18?2, P-value?=?0.05) on CHD, as suggested by Mendelian randomization analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_provenance.
- NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_assertion evidence source_evidence_literature NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_provenance.
- NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_assertion SIO_000772 25502724 NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_provenance.
- NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_assertion wasDerivedFrom befree-2016 NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_provenance.
- NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_assertion wasGeneratedBy ECO_0000203 NP1247778.RAmVgHZJUOKnxVJXtUvW1rCaHdKncryMyy9VEX0hTeZyE130_provenance.