Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_provenance.
- NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_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." NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_provenance.
- NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_assertion evidence source_evidence_literature NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_provenance.
- NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_assertion SIO_000772 18335162 NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_provenance.
- NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_assertion wasDerivedFrom befree-20140225 NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_provenance.
- NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_assertion wasGeneratedBy ECO_0000203 NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP258643.RAPtL9LpEh23gNUpBZOcXmL2Z54SUJQ-7SI31xWU_VWoc130_provenance.