Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_assertion type Assertion NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_head.
- NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_assertion wasGeneratedBy ECO_0000203 NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_provenance.
- NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_assertion wasDerivedFrom befree-20140225 NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_provenance.
- NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_assertion SIO_000772 17847002 NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_provenance.
- NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_assertion evidence source_evidence_literature NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_provenance.
- NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_assertion description "[This extensive study, involving multiple independent populations, provides the first evidence that genetic variants in LRP8 may contribute to the development of premature and familial CAD and MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP659143.RA1n_miYFSH547KgEBVJdvfYGJbS6H0uge1jjo7sPublA130_provenance.