Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP234862.RAfdirim2qx4XXtVunPiVWvhfJUJAlYADr-4KC5pE4YTI130_provenance.