Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_provenance.
- NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_assertion description "[Given that the switch from G to T in SNP rs3791878 might cause the loss of ARNT and XBP1 transcriptional factor binding sites using a bioinformatics approach, our positive findings of this SNP support the hypothesis that the abruption of GAD1 gene is important to the risk of schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_provenance.
- NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_assertion evidence source_evidence_literature NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_provenance.
- NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_assertion SIO_000772 18335162 NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_provenance.
- NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_assertion wasDerivedFrom befree-2016 NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_provenance.
- NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_assertion wasGeneratedBy ECO_0000203 NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_provenance.
- befree-2016 importedOn "2016-02-19" NP660101.RAyOpbJT7WlS0xoDe9UE3lKN30IWW64-GqK47_v_atasA130_provenance.