Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_provenance.
- NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_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." NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_provenance.
- NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_assertion evidence source_evidence_literature NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_provenance.
- NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_assertion SIO_000772 17994190 NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_provenance.
- NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_assertion wasDerivedFrom befree-20140225 NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_provenance.
- NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_assertion wasGeneratedBy ECO_0000203 NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP177575.RAt-a_gYNbd3ZCcv_8R-i-SXlDkwG0lCnDTtYCEeLzNwA130_provenance.