Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_provenance.
- NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_assertion description "[Here, a detailed survey of genetic variation in the ABCA1 region has been performed in a total of 1,567 Swedish dementia cases (including 1,275 with Alzheimer disease) and 2,203 controls, providing evidence of association with maximum significance at marker rs2230805 (odds ratio [OR]=1.39; 95% confidence interval [CI] 1.23-1.57, p=7.7x10(-8)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_provenance.
- NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_assertion evidence source_evidence_literature NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_provenance.
- NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_assertion SIO_000772 19606474 NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_provenance.
- NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_assertion wasDerivedFrom befree-2016 NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_provenance.
- NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_assertion wasGeneratedBy ECO_0000203 NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_provenance.
- befree-2016 importedOn "2016-02-19" NP751550.RAoGnnXoIDtgG7-AJjVV-mmiJZd0uM_5CRVWvPFUrWlug130_provenance.