Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_provenance.
- NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_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." NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_provenance.
- NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_assertion evidence source_evidence_literature NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_provenance.
- NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_assertion SIO_000772 12452480 NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_provenance.
- NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_assertion wasDerivedFrom befree-20140225 NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_provenance.
- NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_assertion wasGeneratedBy ECO_0000203 NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP204672.RAjWvFXlW6z4aHjqUecC27Ubg6t0184UCEztpL4RK1m4M130_provenance.