Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_provenance.
- NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_assertion description "[KCNQ1 is associated with two different entities of LQTS, the autosomal-dominant Romano-Ward syndrome (RWS), and the autosomal-recessive Jervell and Lange-Nielsen syndrome (JLNS) characterized by bilateral deafness in addition to cardiac arrhythmias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_provenance.
- NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_assertion evidence source_evidence_literature NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_provenance.
- NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_assertion SIO_000772 15950200 NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_provenance.
- NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_assertion wasDerivedFrom befree-20140225 NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_provenance.
- NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_assertion wasGeneratedBy ECO_0000203 NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP649135.RAYziULy1YMDfuc9GWWb-Lu2ojXkMSRf0g3zUapCgo9Lg130_provenance.