Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_assertion> ?p ?o ?g. }
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- NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_assertion type Assertion NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_head.
- NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_assertion description "[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_provenance.
- NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_assertion evidence source_evidence_literature NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_provenance.
- NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_assertion SIO_000772 19565319 NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_provenance.
- NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_assertion wasDerivedFrom befree-20150227 NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_provenance.
- NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_assertion wasGeneratedBy ECO_0000203 NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_provenance.