Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_provenance.
- NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_assertion description "[We examined three polymorphisms in the dopamine D2 receptor gene (DRD2), two sites in the 3' region of the dopamine transporter (DAT) gene, two sites in the promoter and coding region of the dopamine D4 (DRD4) receptor gene, as well as polymorphic sites in the serotonin 6 receptor gene, the serotonin transporter gene and the tryptophan hydroxylase gene, for association with TD susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_provenance.
- NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_assertion evidence source_evidence_literature NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_provenance.
- NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_assertion SIO_000772 14583797 NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_provenance.
- NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_assertion wasDerivedFrom befree-20140225 NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_provenance.
- NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_assertion wasGeneratedBy ECO_0000203 NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_provenance.
- befree-20140225 importedOn "2014-02-25" NP290394.RAIB8_i1iYtIp7zqWjj2h_USmUQXci7bZxMCjs54kig68130_provenance.