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- NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_assertion type Assertion NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_head.
- NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_assertion description "[Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_provenance.
- NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_assertion evidence source_evidence_literature NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_provenance.
- NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_assertion SIO_000772 24571113 NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_provenance.
- NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_assertion wasDerivedFrom befree-20150227 NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_provenance.
- NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_assertion wasGeneratedBy ECO_0000203 NP682498.RAJcYShcerubT71RJ7lOWTcCmzc5c269zKJsR4ht24xuA130_provenance.