Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_provenance.
- NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_assertion description "[While the ACE I/D, AT1R A1166C, and PAI-1 4G/5G did not contribute to the genetic susceptibility to vascular dementia (P>0.05), a significant association with vascular dementia was shown in the T235M polymorphism of AGT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_provenance.
- NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_assertion evidence source_evidence_literature NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_provenance.
- NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_assertion SIO_000772 16603315 NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_provenance.
- NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_assertion wasDerivedFrom befree-20140225 NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_provenance.
- NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_assertion wasGeneratedBy ECO_0000203 NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP190797.RAylNadkyDSQRPD1_pXtGAvC9fJTjUsbVUUGhQWa4yeC4130_provenance.