Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_assertion> ?p ?o ?g. }
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- NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_assertion type Assertion NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_head.
- NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_assertion description "[In this longitudinal study of adolescents with 22q11.2 deletion syndrome, we identified the catechol-O-methyltransferase low-activity allele (COMT(L)) as a risk factor for decline in prefrontal cortical volume and cognition, as well as for the consequent development of psychotic symptoms during adolescence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_provenance.
- NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_assertion evidence source_evidence_literature NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_provenance.
- NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_assertion SIO_000772 16234808 NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_provenance.
- NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_assertion wasDerivedFrom befree-2016 NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_provenance.
- NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_assertion wasGeneratedBy ECO_0000203 NP518609.RAb5bH_g1EpWof0du_eNCzI5dSkbA8LziH6k3HCnJSgCI130_provenance.