Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_provenance.
- NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_assertion description "[Sequence variants of ACE, AGT, AT1R, and PAI-1 as genetic risk factors for vascular dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_provenance.
- NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_assertion evidence source_evidence_literature NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_provenance.
- NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_assertion SIO_000772 16603315 NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_provenance.
- NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_assertion wasDerivedFrom gad-20150221 NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_provenance.
- NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_assertion wasGeneratedBy ECO_0000203 NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP82515.RAm-ymHMTMUtub1ZDR_92No4K5vhWQuLmH5HSAe6v_SNM130_provenance.