Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_assertion type Assertion NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_head.
- NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_assertion description "[Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_provenance.
- NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_assertion evidence source_evidence_literature NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_provenance.
- NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_assertion SIO_000772 16542388 NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_provenance.
- NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_assertion wasDerivedFrom gad-20150221 NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_provenance.
- NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_assertion wasGeneratedBy ECO_0000203 NP99512.RASuFwg0q-DG8LrytNP4bQ8YFFfNA4LENHgmsNsTKOxnI130_provenance.