Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_provenance.
- NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_assertion description "[Mutation at SCA6 was also the most common form of sporadic SCA at 11%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_provenance.
- NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_assertion evidence source_evidence_literature NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_provenance.
- NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_assertion SIO_000772 11359084 NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_provenance.
- NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_assertion wasDerivedFrom befree-2016 NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_provenance.
- NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_assertion wasGeneratedBy ECO_0000203 NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_provenance.
- befree-2016 importedOn "2016-02-19" NP318402.RAdYe37CzAx8bV55zRriy7fKD0-S_myJNtaMZkGcUYTOA130_provenance.