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- NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_assertion type Assertion NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_head.
- NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_assertion wasGeneratedBy ECO_0000203 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 SIO_000772 23429546 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 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.