Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_assertion type Assertion NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_head.
- NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_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." NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_provenance.
- NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_assertion evidence source_evidence_literature NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_provenance.
- NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_assertion SIO_000772 16234808 NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_provenance.
- NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_assertion wasDerivedFrom befree-20140225 NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_provenance.
- NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_assertion wasGeneratedBy ECO_0000203 NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_provenance.