Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_provenance.
- NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_assertion description "[The DDX11-deficient patient represents another cohesinopathy, besides Cornelia de Lange syndrome and Roberts syndrome, and shows that DDX11 functions at the interface between DNA repair and sister chromatid cohesion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_provenance.
- NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_assertion evidence source_evidence_literature NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_provenance.
- NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_assertion SIO_000772 20137776 NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_provenance.
- NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_assertion wasDerivedFrom befree-20140225 NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_provenance.
- NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_assertion wasGeneratedBy ECO_0000203 NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_provenance.
- befree-20140225 importedOn "2014-02-25" NP789638.RABCYLn4wr59VjPxD77Oez6GDvu5y-XJ6VP4TrbxYvEek130_provenance.