Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_provenance.
- NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_assertion description "[A cerebellar X-linked human ataxia has recently been found to be caused by a mutation in the calmodulin-binding domain of PMCA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_provenance.
- NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_assertion evidence source_evidence_literature NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_provenance.
- NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_assertion SIO_000772 23413890 NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_provenance.
- NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_assertion wasDerivedFrom befree-20150227 NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_provenance.
- NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_assertion wasGeneratedBy ECO_0000203 NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP278694.RAvPbgGBLfaiXaO3vI2Cj9AKcXqptJx8z1wySjwvDK7yk130_provenance.