Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_provenance.
- NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_assertion wasGeneratedBy ECO_0000203 NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_provenance.
- NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_assertion wasDerivedFrom befree-20140225 NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_provenance.
- NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_assertion SIO_000772 22981886 NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_provenance.
- NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_assertion evidence source_evidence_literature NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_provenance.
- NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_assertion description "[None of the SNPs showed a significant association with MDD, but a SNP (rs2075984) in CSNK1E and SNP (rs6502097) in CSNK1D were associated with SCZ (P=0.0091, uncorrected) and BD (P=0.030, uncorrected), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP784196.RAsbsk8pH5tMWxCeKIfGNL9YWa1y4eeMPAxPb9rmWtqOE130_provenance.