Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_assertion> ?p ?o ?g. }
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- NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_assertion type Assertion NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_head.
- NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_assertion description "[Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_provenance.
- NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_assertion evidence source_evidence_literature NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_provenance.
- NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_assertion SIO_000772 23910792 NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_provenance.
- NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_assertion wasDerivedFrom befree-2016 NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_provenance.
- NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_assertion wasGeneratedBy ECO_0000203 NP1099035.RATm8rrLngiuHuUrGIn0r7BSodvGrSDPfn7w5ZD3L5iIU130_provenance.