@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:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_head { this: np:hasAssertion dgn-np:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_assertion; np:hasProvenance dgn-np:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_provenance; np:hasPublicationInfo dgn-np:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_publicationInfo; a np:Nanopublication . dgn-np:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_assertion a np:Assertion . dgn-np:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_provenance a np:Provenance . dgn-np:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_publicationInfo a np:PublicationInfo . } dgn-np:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_assertion { miriam-gene:1312 a ncit:C16612 . lld:C0220704 a ncit:C7057 . dgn-gda:DGNb15c30554bddc7b207b1896db631c5f9 sio:SIO_000628 miriam-gene:1312, lld:C0220704; a sio:SIO_001121 . } dgn-np:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_provenance { dgn-np:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_assertion dcterms:description "[The gene for COMT is located on chromosome 22q11, an area that has been implicated in the pathogenesis of schizophrenia through linkage studies and through the detection of deletions in schizophrenics and velocardiofacial syndrome patients that often present psychotic symptomatology.]. 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:12192614; 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:NP365378.RAAnPQe1NbjCAAu2Jq_yyfQZtGM17xu4zfEeljMAnGiP4130_publicationInfo { this: dcterms:created "2016-05-13T12:44:31+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" . }