Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_assertion type Assertion NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_head.
- NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_assertion wasGeneratedBy ECO_0000203 NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_provenance.
- NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_assertion wasDerivedFrom befree-2016 NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_provenance.
- NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_assertion SIO_000772 12395102 NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_provenance.
- NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_assertion evidence source_evidence_literature NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_provenance.
- NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_assertion description "[Mutations in the voltage-gated potassium channel genes KCNQ2 and KCNQ3 have been found to cause benign familial neonatal convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372138.RAiPkMR5fkldMjB-DRlCtYG0mQUwhrXF6uNECaPmtQEEU130_provenance.