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- source_evidence_literature type ECO_0000212 NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_provenance.
- NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_assertion description "[It was postulated that genetic variations in SCNN1A could lead to an increased risk of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_provenance.
- NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_assertion evidence source_evidence_literature NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_provenance.
- NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_assertion SIO_000772 11752024 NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_provenance.
- NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_assertion wasDerivedFrom befree-20140225 NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_provenance.
- NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_assertion wasGeneratedBy ECO_0000203 NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP676894.RA-wMXQaRINV3h_3hLwyecac1wdF8EzeAtcvCbQASPEOs130_provenance.