Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_assertion type Assertion NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_head.
- NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_assertion description "[Mutations in the KCNQ1, HERG, SCN5A, minK and MiRP1 genes cause long QT syndrome (LQTS), of which there are two forms: the Romano Ward syndrome and the Jervell and Lange-Nielsen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_provenance.
- NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_assertion evidence source_evidence_literature NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_provenance.
- NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_assertion SIO_000772 18752142 NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_provenance.
- NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_assertion wasDerivedFrom gad-20150221 NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_provenance.
- NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_assertion wasGeneratedBy ECO_0000203 NP65016.RAAuDvztZVAn5yrnBi1kU0HhnMYIjLkUMpOE2iGMRwr4s130_provenance.