@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:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_head { this: np:hasAssertion dgn-np:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_assertion; np:hasProvenance dgn-np:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_provenance; np:hasPublicationInfo dgn-np:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_publicationInfo; a np:Nanopublication . dgn-np:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_assertion a np:Assertion . dgn-np:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_provenance a np:Provenance . dgn-np:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_assertion { miriam-gene:1565 a ncit:C16612 . lld:C0392156 a ncit:C7057 . dgn-gda:DGN77fdbbee667e73e22ae25a9262867072 sio:SIO_000628 miriam-gene:1565, lld:C0392156; a sio:SIO_001121 . } dgn-np:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_provenance { dgn-np:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_assertion dcterms:description "[There were no statistically significant differences between the group of PMs and the group of patients with at least one functional CYP2D6 allele in view of patient's characteristics or any of the items of the AIMS, the SAS or the Barnes Akathisia Scale.]. 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:16478753; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP342512.RAr-_sqX0eSx82TO5vty8D59fP7wGPrgAyU3RiRJjjVqQ130_publicationInfo { this: dcterms:created "2015-08-25T14:40:57+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }