@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:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_head { this: np:hasAssertion dgn-np:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_assertion; np:hasProvenance dgn-np:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_provenance; np:hasPublicationInfo dgn-np:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_publicationInfo; a np:Nanopublication . dgn-np:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_assertion a np:Assertion . dgn-np:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_provenance a np:Provenance . dgn-np:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_publicationInfo a np:PublicationInfo . } dgn-np:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_assertion { miriam-gene:4544 a ncit:C16612 . lld:C0917799 a ncit:C7057 . dgn-gda:DGN3cafee5ebf0afa69e5d9ff9bc08a1373 sio:SIO_000628 miriam-gene:4544, lld:C0917799; a sio:SIO_001121 . } dgn-np:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_provenance { dgn-np:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_assertion dcterms:description "[In this study, we investigated whether single nucleotide polymorphisms (SNPs) in the promoter region of the melatonin receptor genes (MTNR1A and MTNR1B) were associated with schizophrenia and with sleep problems such as insomnia and hypersomnia in schizophrenia patients.]. 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:21526376; 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:NP890167.RAJUSB28onmAWLcpsLirKAmBRd-rYGn0CDec0FttpeeXA130_publicationInfo { this: dcterms:created "2016-05-13T12:48:28+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" . }