Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_assertion> ?p ?o ?g. }
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- NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_assertion type Assertion NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_head.
- NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_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." NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_provenance.
- NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_assertion evidence source_evidence_literature NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_provenance.
- NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_assertion SIO_000772 19565319 NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_provenance.
- NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_assertion wasDerivedFrom befree-20140225 NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_provenance.
- NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_assertion wasGeneratedBy ECO_0000203 NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_provenance.