Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance.
- NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance.
- NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_assertion evidence source_evidence_literature NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance.
- NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_assertion SIO_000772 23429546 NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance.
- NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_assertion wasDerivedFrom befree-20150227 NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance.
- NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_assertion wasGeneratedBy ECO_0000203 NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance.