Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_provenance.
- NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_assertion wasGeneratedBy ECO_0000203 NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_provenance.
- NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_assertion wasDerivedFrom befree-20140225 NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_provenance.
- NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_assertion SIO_000772 22306195 NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_provenance.
- NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_assertion evidence source_evidence_literature NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_provenance.
- NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_assertion description "[In order to find the causal variants of NRGN gene in schizophrenia, we searched for genetic variants in the promoter region and all the exons (including both UTR ends and rs12807809) using direct sequencing in a sample of patients with schizophrenia (n=346) and non-psychotic controls (n=345), both being Han Chinese from Taiwan, and conducted an association and functional study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_provenance.
- befree-20140225 importedOn "2014-02-25" NP425174.RAeP5hyifXIR1x7984iRmkemy_tfuE8m40nxdnN7LV-Ew130_provenance.