Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_assertion> ?p ?o ?g. }
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- NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_assertion type Assertion NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_head.
- NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_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." NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_provenance.
- NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_assertion evidence source_evidence_literature NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_provenance.
- NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_assertion SIO_000772 24571113 NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_provenance.
- NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_assertion wasDerivedFrom befree-20150227 NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_provenance.
- NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_assertion wasGeneratedBy ECO_0000203 NP682436.RAg8vSIRFiZp7TRlwpU8TcVW1Aw--FTQV5CGs2u5AHREo130_provenance.