Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_provenance.
- NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_assertion description "[Results do not support the hypothesis that common variants in the SLC6A2 and COMT genes in particular are associated with ADHD, but might give some evidence for interactive effects between these gene variants on ADHD severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_provenance.
- NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_assertion evidence source_evidence_literature NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_provenance.
- NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_assertion SIO_000772 17994190 NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_provenance.
- NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_assertion wasDerivedFrom befree-2016 NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_provenance.
- NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_assertion wasGeneratedBy ECO_0000203 NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_provenance.
- befree-2016 importedOn "2016-02-19" NP639717.RAbJr6ZfeYIPNY1S0Q5RciEuYZknXoLYHCoFLy3I_Jt8s130_provenance.