Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_provenance.
- NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_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 i]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_provenance.
- NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_assertion evidence source_evidence_literature NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_provenance.
- NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_assertion SIO_000772 20691829 NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_provenance.
- NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_assertion wasDerivedFrom gad-20150221 NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_provenance.
- NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_assertion wasGeneratedBy ECO_0000203 NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP183351.RAiUMqlHu-wvilw26mvuX8gkfFj4lT3IN-dbHZ2fWfCU4130_provenance.