Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance.
- NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion description "[The results of karyotypic, clinical, and ERP investigations of this family suggest that the recently described genes DISC1 and DISC2, which are directly disrupted by the breakpoint on chromosome 1, may have a role in the development of a disease phenotype that includes schizophrenia as well as unipolar and bipolar affective disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance.
- NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion evidence source_evidence_literature NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance.
- NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion SIO_000772 11443544 NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance.
- NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion wasDerivedFrom befree-20140225 NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance.
- NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion wasGeneratedBy ECO_0000203 NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance.