Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_provenance.
- NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_assertion description "[Caucasian non-Hispanic participants in the STAR*D study of treatment for depression for whom DNA was available (N = 1213) were genotyped at two single-nucleotide polymorphisms (SNPs) (rs10848635 and rs1006737) in the CACNA1C gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_provenance.
- NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_assertion evidence source_evidence_literature NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_provenance.
- NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_assertion SIO_000772 19388002 NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_provenance.
- NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_assertion wasDerivedFrom befree-2016 NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_provenance.
- NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_assertion wasGeneratedBy ECO_0000203 NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_provenance.
- befree-2016 importedOn "2016-02-19" NP734248.RAKvGFVwS3RmwcQtEchMyvnuoV4WlhziJhff5LB9Yphhc130_provenance.