@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_head { this: np:hasAssertion dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_assertion; np:hasProvenance dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_provenance; np:hasPublicationInfo dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_publicationInfo; a np:Nanopublication . dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_assertion a np:Assertion . dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_provenance a np:Provenance . dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_publicationInfo a np:PublicationInfo . } dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_assertion { miriam-gene:1815 a ncit:C16612 . lld:C0036341 a ncit:C7057 . dgn-gda:DGNcbd86898564293720a57b025cac9a5b7 sio:SIO_000628 miriam-gene:1815, lld:C0036341; a sio:SIO_001122 . } dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_provenance { dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_assertion dcterms:description "[To elucidate main effects of dopamine receptor D4 (DRD4) and cathecol-O-methyltransferase (COMT) genes as well as their interaction effect on neurocognitive traits, DRD4 gene polymorphisms (-809G/A, -521C/T) and the COMT gene Val158Met polymorphism, along with characteristics of verbal memory, executive functions and peculiarities of associative processes, have been studied in 150 patients with schizophrenia, 83 their relatives and 118 mentally healthy subjects without positive family history of psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:16921721; prov:wasDerivedFrom dgn-void:gad-20130706; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP45286.RAz3NxyH1ZkCMa1XADbV6eV8tK0LhwSUZPZCDfjJj0j-c130_publicationInfo { this: dcterms:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }