Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_provenance.
- NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_assertion description "[We performed a genetic association study using four functional polymorphisms of the dopamine receptor 4 (DRD4), dopamine transporter (DAT), mono-amino-oxidase A (MAOA) and cathecol-O-methyl-transferase (COMT) genes in 103 patients with chronic daily headache associated with DA (CDHDA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_provenance.
- NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_assertion evidence source_evidence_literature NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_provenance.
- NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_assertion SIO_000772 16930369 NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_provenance.
- NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_assertion wasDerivedFrom befree-20140225 NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_provenance.
- NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_assertion wasGeneratedBy ECO_0000203 NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP626238.RAulzhK53aRkn2HYbiPmCVvMdEAEC4NdGXVr4G2mQihm4130_provenance.