Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_provenance.
- NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_assertion description "[genetic variation in the ALOX5AP gene contributes to CHD risk in patients with FH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_provenance.
- NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_assertion evidence source_evidence_literature NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_provenance.
- NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_assertion SIO_000772 18775537 NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_provenance.
- NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_assertion wasDerivedFrom gad-20150221 NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_provenance.
- NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_assertion wasGeneratedBy ECO_0000203 NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP106130.RA4G6hbpFW9fSYtbFE05HXImcRscMCAn2LHQxl0BNeNLg130_provenance.