Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_provenance.
- NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_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." NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_provenance.
- NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_assertion evidence source_evidence_literature NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_provenance.
- NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_assertion SIO_000772 15670397 NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_provenance.
- NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_assertion wasDerivedFrom gad-20150221 NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_provenance.
- NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_assertion wasGeneratedBy ECO_0000203 NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90266.RAokOJScloNz8B3jKGSMkpFobIqEGdLJNbzwp_KT-_aKw130_provenance.