Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_provenance.
- NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_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." NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_provenance.
- NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_assertion evidence source_evidence_literature NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_provenance.
- NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_assertion SIO_000772 18335162 NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_provenance.
- NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_assertion wasDerivedFrom befree-20150227 NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_provenance.
- NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_assertion wasGeneratedBy ECO_0000203 NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP778852.RA3CPsZwcgm5PWZ3RLbCUyQM2DJSngF0ze2Qv91-gLzWs130_provenance.