Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_provenance.
- NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_assertion description "[Increased coassembly of NR2B and NR1 with PSD-95 may underlie one of the cellular mechanisms that contributes to in situ increased hyperexcitability, leading to seizure generation in focal cortical dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_provenance.
- NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_assertion evidence source_evidence_literature NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_provenance.
- NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_assertion SIO_000772 15030493 NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_provenance.
- NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_assertion wasDerivedFrom lhgdn-20090331 NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_provenance.
- NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_assertion wasGeneratedBy ECO_0000203 NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP214239.RAmW635Hv5tfhI3qvMY93-qJr_Z3x3iFWFamAnGT_gxZI130_provenance.