Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance.
- NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance.
- NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_assertion evidence source_evidence_literature NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance.
- NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_assertion SIO_000772 16302874 NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance.
- NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_assertion wasDerivedFrom befree-20140225 NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance.
- NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_assertion wasGeneratedBy ECO_0000203 NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance.