Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_provenance.
- NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_assertion description "[It has been suggested that polymorphisms at the genes for presenilin-1 (PS-1) and alpha-1-antichymotrypsin (ACT) confer an increased risk for AD in the general population, and therefore potentially to AD in people with DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_provenance.
- NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_assertion evidence source_evidence_literature NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_provenance.
- NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_assertion SIO_000772 10581479 NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_provenance.
- NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_assertion wasDerivedFrom befree-2016 NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_provenance.
- NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_assertion wasGeneratedBy ECO_0000203 NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_provenance.
- befree-2016 importedOn "2016-02-19" NP268794.RABFhqGCot4I_MhSXTMe66yWwm2Hgh6MFhRx8KZT2Tg5g130_provenance.