Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_provenance.
- NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_assertion description "[The goal of this study was to investigate the genotype-to-phenotype relationship between SCN5A gene mutation and progressive cardiac conduction defect in order to gain insights into the pathophysiologic mechanisms of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_provenance.
- NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_assertion evidence source_evidence_literature NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_provenance.
- NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_assertion SIO_000772 12598077 NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_provenance.
- NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_assertion wasDerivedFrom befree-20140225 NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_provenance.
- NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_assertion wasGeneratedBy ECO_0000203 NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP417629.RADVvwBtGCDlZtKRoSt-p9YcZvFJxJ5uq3NTdX05hNzE0130_provenance.