Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_provenance.
- NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_assertion description "[This unifying connection depends, at least in part, on redox sensor NAD(+)-dependent deacetylase, Sirt1, and a NF-?B-dependent p65 and RelB feed-forward and gene-specific pathway that generates silent facultative heterochromatin and active euchromatin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_provenance.
- NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_assertion evidence source_evidence_literature NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_provenance.
- NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_assertion SIO_000772 21610199 NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_provenance.
- NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_assertion wasDerivedFrom befree-20140225 NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_provenance.
- NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_assertion wasGeneratedBy ECO_0000203 NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP482789.RAqm9HiSXRHLXMzbt5iEWd7AC_qJE_C3NWOmiO_aZgn7A130_provenance.