Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_provenance.
- NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_assertion description "[Although an association of these polymorphisms with the appearance of CAD and MI have been published before, our results strongly argue against a relevant role of the (GT)n repeat or the -413A>T SNP in the HMOX1 promoter in CAD or MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_provenance.
- NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_assertion evidence source_evidence_literature NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_provenance.
- NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_assertion SIO_000772 19389234 NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_provenance.
- NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_assertion wasDerivedFrom gad-20150221 NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_provenance.
- NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_assertion wasGeneratedBy ECO_0000203 NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP73618.RAxPFG8TfHGk-OXdKdxIbOaTjrkmjV42-PcAnyosUDov0130_provenance.