Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_assertion> ?p ?o ?g. }
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- NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_assertion type Assertion NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_head.
- NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_assertion description "[A simple genetic score of 11 polymorphisms may identify those subjects at increased risk of CHD beyond conventional risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_provenance.
- NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_assertion evidence source_evidence_literature NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_provenance.
- NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_assertion SIO_000772 19501493 NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_provenance.
- NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_assertion wasDerivedFrom gad-20130706 NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_provenance.
- NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_assertion wasGeneratedBy ECO_0000203 NP81830.RA9vpLrd07tP_NyfEGnoyoblwHzbFQYIHJ9XiMhd-RbUo130_provenance.