Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_provenance.
- NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_assertion description "[Although initially thought to be within the same spectrum as severe myoclonic epilepsy of infancy, the exclusion of SCN1A mutations in non-generalized epilepsy with febrile seizures plus (GEFS+) MAE cases has confirmed the genetic distinction of MAE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_provenance.
- NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_assertion evidence source_evidence_literature NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_provenance.
- NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_assertion SIO_000772 22780699 NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_provenance.
- NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_assertion wasDerivedFrom befree-20140225 NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_provenance.
- NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_assertion wasGeneratedBy ECO_0000203 NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP746063.RACZSEkSYDvmTNT3cLkv9HPvoLnO_y2xUTQIXgUOZORhk130_provenance.