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- source_evidence_literature type ECO_0000212 NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_provenance.
- NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_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." NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_provenance.
- NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_assertion evidence source_evidence_literature NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_provenance.
- NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_assertion SIO_000772 14583797 NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_provenance.
- NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_assertion wasDerivedFrom gad-20150221 NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_provenance.
- NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_assertion wasGeneratedBy ECO_0000203 NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP82328.RABY1D8DS2ig5pxtbLUhErse2YM5JZBrCfz_evgxmn0BQ130_provenance.