Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_provenance.
- NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_assertion description "[We did not detect pathogenic variants in GRIN2A in other epileptic encephalopathies (n = 475) nor in probands with benign childhood epilepsy with centrotemporal spikes (n = 81).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_provenance.
- NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_assertion evidence source_evidence_literature NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_provenance.
- NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_assertion SIO_000772 23933818 NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_provenance.
- NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_assertion wasDerivedFrom befree-20150227 NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_provenance.
- NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_assertion wasGeneratedBy ECO_0000203 NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434526.RAVwGosJTjvuOewN45K4wnT1W-Gv3S3tgOdNGtoSKtWy0130_provenance.