Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_provenance.
- NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_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." NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_provenance.
- NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_assertion evidence source_evidence_literature NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_provenance.
- NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_assertion SIO_000772 22780699 NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_provenance.
- NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_assertion wasDerivedFrom befree-2016 NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_provenance.
- NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_assertion wasGeneratedBy ECO_0000203 NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_provenance.
- befree-2016 importedOn "2016-02-19" NP996411.RAzW2hI3gqk_rvTnuJ3tJpTE3aQ5Y2dXXvUuER4wz-k-4130_provenance.