Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_provenance.
- NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_assertion description "[Paraoxonase, ACE, and MTHFR polymorphisms were not associated with VD or LOAD; these common polymorphisms might have a marginal role in the pathogenesis of dementia in older subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_provenance.
- NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_assertion evidence source_evidence_literature NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_provenance.
- NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_assertion SIO_000772 11328206 NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_provenance.
- NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_assertion wasDerivedFrom befree-20140225 NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_provenance.
- NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_assertion wasGeneratedBy ECO_0000203 NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP171001.RAAgAd4wO83rfGST5ZKW9JT4eHjfqN5LlTMWcFpNM1q9A130_provenance.