Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_assertion type Assertion NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_head.
- NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_assertion wasGeneratedBy ECO_0000203 NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_provenance.
- NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_assertion wasDerivedFrom befree-20140225 NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_provenance.
- NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_assertion SIO_000772 10898405 NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_provenance.
- NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_assertion evidence source_evidence_literature NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_provenance.
- NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_assertion description "[It is becoming clear that mutations in the KVLQT1, human `ether-a-go-go` related gene, cardiac voltage-dependent sodium channel gene, minK and MiRP1 genes, respectively, are responsible for the LQT1, LQT2, LQT3, LQT5 and LQT6 variants of the Romano-Ward syndrome, characterized by autosomal dominant transmission and no deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237995.RApDOQJPfrkyKfiBXo1ZNcpIAGD5mhdcp15YpIgM6fybs130_provenance.