@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:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_head { this: np:hasAssertion dgn-np:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_assertion; np:hasProvenance dgn-np:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_provenance; np:hasPublicationInfo dgn-np:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_publicationInfo; a np:Nanopublication . dgn-np:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_assertion a np:Assertion . dgn-np:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_provenance a np:Provenance . dgn-np:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_publicationInfo a np:PublicationInfo . } dgn-np:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_assertion { miriam-gene:6531 a ncit:C16612 . lld:C1263846 a ncit:C7057 . dgn-gda:DGNbb0d2ac75d58b361691ef27798126411 sio:SIO_000628 miriam-gene:6531, lld:C1263846; a sio:SIO_001121 . } dgn-np:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_provenance { dgn-np:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_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:NP552942.RAbUpmnVt032a7jT6SwKLk4ABHOvd2OHXXaSDkoM5LdwY130_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" . }