Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_provenance.
- NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_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." NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_provenance.
- NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_assertion evidence source_evidence_literature NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_provenance.
- NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_assertion SIO_000772 18335162 NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_provenance.
- NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_assertion wasDerivedFrom befree-20140225 NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_provenance.
- NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_assertion wasGeneratedBy ECO_0000203 NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_provenance.
- befree-20140225 importedOn "2014-02-25" NP830640.RAEkUFuJsdCvdDQFTxKLR6D5jZnoVFw6Ru1AWrOmMnPek130_provenance.