Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance.
- NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_assertion description "[Recent genetic studies have investigated associations between ICD and polymorphisms of genes involved in the dopamine metabolism pathway (COMT, DAT), dopamine receptors (DRD1, DRD2, DRD3, DRD4), serotonin receptors and its transporter (HTR2A, 5HTT), and glutamate receptors (GRIN2B).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance.
- NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_assertion evidence source_evidence_literature NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance.
- NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_assertion SIO_000772 23232665 NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance.
- NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_assertion wasDerivedFrom befree-20140225 NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance.
- NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_assertion wasGeneratedBy ECO_0000203 NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance.
- befree-20140225 importedOn "2014-02-25" NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance.