Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_provenance.
- NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_assertion description "[To increase SNP coverage to 100% for common variants (m.a.f.>0.1, r(2)>0.8), we selected seven genes from the GAIN-MDD GWAS: PCLO, GZMK, ANPEP, AFAP1L1, ST3GAL6, FGF14 and PTK2B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_provenance.
- NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_assertion evidence source_evidence_literature NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_provenance.
- NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_assertion SIO_000772 22649524 NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_provenance.
- NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_assertion wasDerivedFrom befree-2016 NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_provenance.
- NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_assertion wasGeneratedBy ECO_0000203 NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_provenance.
- befree-2016 importedOn "2016-02-19" NP986223.RA_Fgl_gbkTCHjaXDROyXxb6Q7J10m7mdRdde85cPHzQA130_provenance.