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- source_evidence_literature type ECO_0000212 NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_provenance.
- NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_assertion description "[Suggestive but notable results were (a) gene-based tests suggesting roles for adenylate cyclase 3 (ADCY3, 2p23.3) and galanin (GAL, 11q13.3); published functional evidence relates both of these to MDD and serotonergic signaling; (b) support for the bipolar disorder risk variant SNP rs1006737 in CACNA1C (P=0.020, odds ratio=1.10); and (c) lack of support for rs2251219, a SNP identified in a meta-analysis of affective disorder studies (P=0.51).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_provenance.
- NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_assertion evidence source_evidence_literature NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_provenance.
- NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_assertion SIO_000772 21042317 NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_provenance.
- NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_assertion wasDerivedFrom befree-2016 NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_provenance.
- NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_assertion wasGeneratedBy ECO_0000203 NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_provenance.
- befree-2016 importedOn "2016-02-19" NP849753.RA7Emk2rR4VLDLJ0FEDYihSBqcNWux7_k2InrL3N4KFSM130_provenance.