Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_provenance.
- NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_assertion description "[In the present case-control study we investigated possible associations between PD phenotype and five candidate polymorphisms including 5-HT transporter (5-HTTLPR and VNTR), monoamine oxidase A (MAOA promoter region), tryptophan hydroxylase 1 (TPH1 218A/C) and 5-HT1B receptor (5-HT1BR 861G/C) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_provenance.
- NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_assertion evidence source_evidence_literature NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_provenance.
- NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_assertion SIO_000772 15670397 NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_provenance.
- NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_assertion wasDerivedFrom gad-20150221 NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_provenance.
- NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_assertion wasGeneratedBy ECO_0000203 NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP63840.RADqoG5vT9MYoJ6YVfE54cUKRXs-nSUWO_Cqm7fU52No8130_provenance.