Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_provenance.
- NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_assertion description "[(3) Levels of SCN9A mRNA specifically are predominant in MAT-LyLu and PC-3 cells; thus, SCN9A is highly likely to be the main source of the functional VGSC detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_provenance.
- NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_assertion evidence source_evidence_literature NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_provenance.
- NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_assertion SIO_000772 11494332 NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_provenance.
- NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_assertion wasDerivedFrom befree-2016 NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_provenance.
- NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_assertion wasGeneratedBy ECO_0000203 NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_provenance.
- befree-2016 importedOn "2016-02-19" NP326575.RABsqCIMRYog9m3HvYTEMT6o8AEoVAncqiYnT8QqUOTbs130_provenance.