Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_provenance.
- NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_assertion description "[Mutations in PRKAG2, the gene for the gamma 2 regulatory subunit of AMP-activated protein kinase, cause cardiac hypertrophy and electrophysiologic abnormalities, particularly preexcitation (Wolff-Parkinson-White syndrome) and atrioventricular conduction block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_provenance.
- NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_assertion evidence source_evidence_literature NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_provenance.
- NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_assertion SIO_000772 11827995 NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_provenance.
- NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_assertion wasDerivedFrom befree-20140225 NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_provenance.
- NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_assertion wasGeneratedBy ECO_0000203 NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_provenance.
- befree-20140225 importedOn "2014-02-25" NP799193.RAxwgmtBZ_kOMOm4AirKk3c1RXbr1R6SvLjwN3NXP_Q58130_provenance.