Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion type Assertion NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_head.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion description "[Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion evidence source_evidence_literature NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion SIO_000772 16958040 NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion wasDerivedFrom befree-2016 NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.
- NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_assertion wasGeneratedBy ECO_0000203 NP568194.RAombomNf1qnYXJGzZE5Cy-dsoA5V47c1CFOA1gWNh1vw130_provenance.