Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_provenance.
- NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_assertion description "[Our results suggest that DNA methylation of such genes as gria2 mediates persistent epileptiform activity and inter-individual differences in the epileptic response to neuronal insult and that pharmacological agents that block DNA methylation inhibit epileptiform activity raising the prospect of DNA methylation inhibitors in epilepsy therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_provenance.
- NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_assertion evidence source_evidence_literature NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_provenance.
- NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_assertion SIO_000772 24098468 NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_provenance.
- NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_assertion wasDerivedFrom befree-20150227 NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_provenance.
- NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_assertion wasGeneratedBy ECO_0000203 NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP433794.RAlPeM6CGc5TVS1Q6fApg_fhaV7i4IMpat7NPwnaKvE3s130_provenance.