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- NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_assertion type Assertion NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_head.
- NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_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." NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_provenance.
- NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_assertion evidence source_evidence_literature NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_provenance.
- NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_assertion SIO_000772 24571113 NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_provenance.
- NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_assertion wasDerivedFrom befree-2016 NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_provenance.
- NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_assertion wasGeneratedBy ECO_0000203 NP1158221.RA1AqoNghT5K1TqoRSI1VID_Gl_Cv6o49H3DZN3X_tb7g130_provenance.