Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_provenance.
- NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_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." NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_provenance.
- NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_assertion evidence source_evidence_literature NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_provenance.
- NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_assertion SIO_000772 12452480 NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_provenance.
- NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_assertion wasDerivedFrom gad-20130706 NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_provenance.
- NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_assertion wasGeneratedBy ECO_0000203 NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_provenance.
- gad-20130706 importedOn "2013-07-06" NP56480.RA6KPmU0hOoo3NVPgv2sdMu9g-cyCwsZ1iQ8HHlnTjXXs130_provenance.