Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_assertion> ?p ?o ?g. }
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- NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_assertion type Assertion NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_head.
- NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_assertion description "[De novo mutations in SCN1A in sporadic Dravet syndrome and germline mutations in SCN1A, SCN1B, and SCN2A in generalized epilepsies with febrile seizures plus have unraveled the heterogenous myoclonic epilepsies of infancy and early childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_provenance.
- NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_assertion evidence source_evidence_literature NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_provenance.
- NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_assertion SIO_000772 16302874 NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_provenance.
- NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_assertion wasDerivedFrom befree-20150227 NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_provenance.
- NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_assertion wasGeneratedBy ECO_0000203 NP682669.RAmV1ad817FLknEgQocbUTfVEikonWYZaDqMwgAFf-3Qo130_provenance.