Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_provenance.
- NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_assertion description "[We focused on the overlapping symptoms between CFS and MDD and performed an association study of the functional single-nucleotide polymorphism (SNP) in the DISC1 gene with CFS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_provenance.
- NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_assertion evidence source_evidence_literature NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_provenance.
- NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_assertion SIO_000772 20227423 NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_provenance.
- NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_assertion wasDerivedFrom befree-20150227 NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_provenance.
- NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_assertion wasGeneratedBy ECO_0000203 NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP886814.RAvS1ttM6EHPSO8BLA3ooeT6JRU-u6wYnIoYBZsDPFcCY130_provenance.