@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:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_head { this: np:hasAssertion dgn-np:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_assertion; np:hasProvenance dgn-np:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_provenance; np:hasPublicationInfo dgn-np:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_publicationInfo; a np:Nanopublication . dgn-np:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_assertion a np:Assertion . dgn-np:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_provenance a np:Provenance . dgn-np:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_publicationInfo a np:PublicationInfo . } dgn-np:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_assertion { miriam-gene:1312 a ncit:C16612 . lld:C1263846 a ncit:C7057 . dgn-gda:DGNbd4b92a8ef1bfb94ab22952effe12dd9 sio:SIO_000628 miriam-gene:1312, lld:C1263846; a sio:SIO_001121 . } dgn-np:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_provenance { dgn-np:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_assertion dcterms:description "[Schizophrenia and Attention Deficit Hyperactivity Disorder, which lead to failure of attentional modulation and working memory, introduce significant changes in gamma responses and have significant associations with genetic polymorphisms of dopamine receptor D4 (DRD4), dopamine transporter (DAT), and catechol-O-methyltransferase (COMT).]. 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:16751296; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP552943.RABg4rSFsvo7-0FOXouqd4mnBUcR4KBPAf6aZm3QSKvJI130_publicationInfo { this: dcterms:created "2016-05-13T12:45:55+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }