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- source_evidence_literature type ECO_0000212 NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_provenance.
- NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_assertion description "[we observe significant association with risk for AD and polymorphisms in ACE, CHRNB2, TF, and an as yet uncharacterized locus on chromosome 7p15.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_provenance.
- NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_assertion evidence source_evidence_literature NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_provenance.
- NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_assertion SIO_000772 18830724 NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_provenance.
- NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_assertion wasDerivedFrom gad-20150221 NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_provenance.
- NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_assertion wasGeneratedBy ECO_0000203 NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP130872.RA9ohMCOZWd0rRFbtJs75Z6BdU-GhjC9XXEww0g00gmBo130_provenance.