Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_provenance.
- 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.
- uniprot-2016 importedOn "2016-01-25" NP1465.RA4m3ThY0mg6DOYZhhee-rAqwgXs1HIvFm7jVlWIei9g8130_provenance.