Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_provenance.
- NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_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." NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_provenance.
- NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_assertion evidence source_evidence_literature NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_provenance.
- NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_assertion SIO_000772 19501493 NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_provenance.
- NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_assertion wasDerivedFrom gad-20130706 NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_provenance.
- NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_assertion wasGeneratedBy ECO_0000203 NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP71871.RA4C19rqpQ6gGBHcJZrLCi3B5ScGe2YktXw3wg6VcVnVA130_provenance.