Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_provenance.
- NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_assertion description "[The discovery of the c.1054C>T; p.R352W mutation in the FOXRED1 gene is a further contribution towards resolving the complex puzzle of the genetic basis of human mitochondrial disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_provenance.
- NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_assertion evidence source_evidence_literature NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_provenance.
- NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_assertion SIO_000772 20858599 NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_provenance.
- NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_assertion wasDerivedFrom befree-20150227 NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_provenance.
- NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_assertion wasGeneratedBy ECO_0000203 NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP919201.RAuJATg8lE1MiOicQVIPsaz7ZDj6oK_ov0dpnOad3LZ4M130_provenance.