Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_provenance.
- NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_assertion description "[In conclusion, the Asp298 variant of the eNOS gene may be associated with CSA in HCM patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_provenance.
- NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_assertion evidence source_evidence_literature NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_provenance.
- NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_assertion SIO_000772 15778808 NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_provenance.
- NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_assertion wasDerivedFrom befree-2016 NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_provenance.
- NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_assertion wasGeneratedBy ECO_0000203 NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_provenance.
- befree-2016 importedOn "2016-02-19" NP486177.RAZGKEmcBcCU_Bcio0rahjoc1EWnNluHYRhLbIIaczWVY130_provenance.