Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_provenance.
- NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_assertion description "[The presence of the 677 C to T mutation in the MTHFR gene does not appear to represent a risk factor for development of end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_provenance.
- NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_assertion evidence source_evidence_literature NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_provenance.
- NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_assertion SIO_000772 9264011 NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_provenance.
- NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_assertion wasDerivedFrom befree-2016 NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_provenance.
- NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_assertion wasGeneratedBy ECO_0000203 NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_provenance.
- befree-2016 importedOn "2016-02-19" NP1378960.RAtxliaZ4qU6LYuvd_KNQDO6AmVXBpK8IW4qyPsXw9N14130_provenance.