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- source_evidence_literature type ECO_0000212 NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_provenance.
- NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_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." NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_provenance.
- NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_assertion evidence source_evidence_literature NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_provenance.
- NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_assertion SIO_000772 12452480 NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_provenance.
- NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_assertion wasDerivedFrom befree-20140225 NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_provenance.
- NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_assertion wasGeneratedBy ECO_0000203 NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP589543.RAUe2Vg_JpDqFoC1DaL2bgW8DHwqUJ5ap2rfm4Ho9cR4g130_provenance.