Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_provenance.
- NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_assertion description "[We genotyped three single nucleotide polymorphisms (SNPs) in ANK3 (rs9804190, rs10994336, and rs10761482) in a case-control sample of German descent including 920 patients with schizophrenia, 400 with bipolar affective disorder, 220 patients with unipolar depression according to ICD 10 and 480 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_provenance.
- NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_assertion evidence source_evidence_literature NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_provenance.
- NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_assertion SIO_000772 21702894 NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_provenance.
- NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_assertion wasDerivedFrom befree-20140225 NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_provenance.
- NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_assertion wasGeneratedBy ECO_0000203 NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP181780.RADal4ArK_O_8XbLttIEFMTmOuF3A56J6tcJAgFTardYE130_provenance.