Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_provenance.
- NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_assertion description "[The multifactorial genetic dysfunction in AD includes mutational loci (APP, PS1, PS2) and diverse susceptibility loci (APOE, A2M, AACT, LRP1, IL1A, TNF, ACE, BACE, BCHE, CST3, MTHFR, GSK3B, NOS3) distributed across the human genome, probably converging in common pathogenic mechanisms that lead to premature neuronal death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_provenance.
- NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_assertion evidence source_evidence_literature NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_provenance.
- NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_assertion SIO_000772 12452480 NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_provenance.
- NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_assertion wasDerivedFrom gad-20130706 NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_provenance.
- NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_assertion wasGeneratedBy ECO_0000203 NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_provenance.
- gad-20130706 importedOn "2013-07-06" NP47881.RAEjG2WmXuO0I5WXtT23Q2MwZBW5Vlefgo9HVEAMRPnPY130_provenance.