Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_assertion type Assertion NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_head.
- NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_provenance.
- NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_assertion evidence source_evidence_literature NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_provenance.
- NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_assertion SIO_000772 11739564 NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_provenance.
- NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_assertion wasDerivedFrom befree-2016 NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_provenance.
- NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_assertion wasGeneratedBy ECO_0000203 NP338589.RA1EJx0yWXCycNfhw7-x_-lhD4ekRi992EH9E8H871Geo130_provenance.