Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_provenance.
- NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_assertion description "[In addition to identifying the epsilon4 allele of APOE and related effects, we pinpointed over a dozen potential Alzheimer disease susceptibility genes (ACE, CHRNB2, CST3, ESR1, GAPDHS, IDE, MTHFR, NCSTN, PRNP, PSEN1, TF, TFAM and TNF) with statistically significant allelic summary odds ratios (ranging from 1.11-1.38 for risk alleles and 0.92-0.67 for protective alleles).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_provenance.
- NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_assertion evidence source_evidence_literature NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_provenance.
- NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_assertion SIO_000772 17192785 NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_provenance.
- NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_assertion wasDerivedFrom befree-2016 NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_provenance.
- NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_assertion wasGeneratedBy ECO_0000203 NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_provenance.
- befree-2016 importedOn "2016-02-19" NP586309.RAQ7y24orC1ILyBqtrVGtkwf8bKfAq3b-NBMdTYo6i9Sc130_provenance.