Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_assertion type Assertion NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_head.
- NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_assertion description "[Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_provenance.
- NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_assertion evidence source_evidence_curated NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_provenance.
- NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_assertion SIO_000772 11410597 NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_provenance.
- NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_assertion wasDerivedFrom uniprot-2016 NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_provenance.
- NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_assertion wasGeneratedBy ECO_0000218 NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_provenance.