Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_assertion type Assertion NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_head.
- NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_assertion description "[A genetic risk score based on nine genetic variants independently associated with CAD irrespective of other cardiovascular risk factors was associated with the presence of the disease. Cohort studies are needed to determine whether this genetic risk score]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_provenance.
- NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_assertion evidence source_evidence_literature NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_provenance.
- NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_assertion SIO_000772 20738937 NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_provenance.
- NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_assertion wasDerivedFrom gad-20150221 NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_provenance.
- NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_assertion wasGeneratedBy ECO_0000203 NP149513.RAuQ0submW_eqXmf5My2MmHH2xveUHi2RhWJT-F5we-P0130_provenance.