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- source_evidence_literature type ECO_0000212 NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_provenance.
- befree-2016 importedOn "2016-02-19" NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_provenance.
- NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_assertion wasGeneratedBy ECO_0000203 NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_provenance.
- NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_assertion wasDerivedFrom befree-2016 NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_provenance.
- NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_assertion SIO_000772 21615493 NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_provenance.
- NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_assertion evidence source_evidence_literature NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_provenance.
- NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_assertion description "[Among these variations, we found a splice site mutation in ASMT (IVS5+2T>C) and one stop mutation in MTNR1A (Y170X) - detected exclusively in patients with ADHD - for which biochemical analyses indicated that they abolish the activity of ASMT and MTNR1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896987.RAfCSKRjpPt2I6oqiDl7qMrWHO_bCxxFOz0msMbtqWY6U130_provenance.