Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_provenance.
- NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_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." NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_provenance.
- NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_assertion evidence source_evidence_literature NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_provenance.
- NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_assertion SIO_000772 17482572 NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_provenance.
- NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_assertion wasDerivedFrom befree-20140225 NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_provenance.
- NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_assertion wasGeneratedBy ECO_0000203 NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP867143.RAhk92lMBXKlejForOWYSIUzuHDBoMjgSsQvqvtfLGfFk130_provenance.