Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_assertion type Assertion NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_head.
- NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_assertion description "[Recently, we identified a rare, nonsynonymous Slc6a3 variant that produces the DAT substitution Ala559Val in two male siblings who share a diagnosis of attention-deficit hyperactivity disorder (ADHD), with other studies identifying the variant in subjects with bipolar disorder (BPD) and autism spectrum disorder (ASD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_provenance.
- NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_assertion evidence source_evidence_literature NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_provenance.
- NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_assertion SIO_000772 25331903 NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_provenance.
- NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_assertion wasDerivedFrom befree-2016 NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_provenance.
- NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_assertion wasGeneratedBy ECO_0000203 NP1230947.RAssI2Z-sB3jP8Fj1rK77YHYrOVXVmny7pNOAqUpBaGxI130_provenance.