Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_provenance.
- NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_assertion description "[We identified the missense mutation M520R in the calmodulin binding domain of the Kv7.1 channel from a German family with long QT-syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_provenance.
- NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_assertion evidence source_evidence_literature NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_provenance.
- NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_assertion SIO_000772 17482572 NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_provenance.
- NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_assertion wasDerivedFrom befree-2016 NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_provenance.
- NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_assertion wasGeneratedBy ECO_0000203 NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_provenance.
- befree-2016 importedOn "2016-02-19" NP608334.RAxG9aSLxSMNml3Ut7KUqYG5Q8aN4olwCHx53JCRod9-U130_provenance.