Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_provenance.
- NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_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." NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_provenance.
- NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_assertion evidence source_evidence_literature NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_provenance.
- NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_assertion SIO_000772 15670397 NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_provenance.
- NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_assertion wasDerivedFrom befree-2016 NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_provenance.
- NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_assertion wasGeneratedBy ECO_0000203 NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_provenance.
- befree-2016 importedOn "2016-02-19" NP477917.RAGPLWtP35fnGqiYy7Ydeiy5ai6idjUNy673CAqq7mkXA130_provenance.