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- source_evidence_literature type ECO_0000212 NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_provenance.
- NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_assertion description "[Here we demonstrate that about 20% of cases of LKS, CSWSS and electroclinically atypical rolandic epilepsy often associated with speech impairment can have a genetic origin sustained by de novo or inherited mutations in the GRIN2A gene (encoding the N-methyl-D-aspartate (NMDA) glutamate receptor ?2 subunit, GluN2A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_provenance.
- NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_assertion evidence source_evidence_literature NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_provenance.
- NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_assertion SIO_000772 23933820 NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_provenance.
- NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_assertion wasDerivedFrom befree-20150227 NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_provenance.
- NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_assertion wasGeneratedBy ECO_0000203 NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434529.RAgl-2OETmjToMx0WfWOJWqBT40fTo78ZESEnvPay5W5w130_provenance.