Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_provenance.
- NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_assertion description "[The Intermountain Healthcares Coronary Genetics study demonstrates the ability of a multigenic, multipathway GRS to improve discrimination of angiographic CAD. Genetic risk scores promise to increase understanding of the genetic basis of CAD and improve identification of individuals at increased CAD risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_provenance.
- NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_assertion evidence source_evidence_literature NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_provenance.
- NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_assertion SIO_000772 20691829 NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_provenance.
- NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_assertion wasDerivedFrom gad-20130706 NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_provenance.
- NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_assertion wasGeneratedBy ECO_0000203 NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP85607.RAFbqAt20DK9Xk0tioWeK0Sfyi4t51RBtix56LzE-tHIg130_provenance.