@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:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_head { this: np:hasAssertion dgn-np:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_assertion; np:hasProvenance dgn-np:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_provenance; np:hasPublicationInfo dgn-np:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_publicationInfo; a np:Nanopublication . dgn-np:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_assertion a np:Assertion . dgn-np:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_provenance a np:Provenance . dgn-np:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_publicationInfo a np:PublicationInfo . } dgn-np:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_assertion { miriam-gene:27185 a ncit:C16612 . lld:C0036341 a ncit:C7057 . dgn-gda:DGNe7053d14b62a22b3d4575209025d855c sio:SIO_000628 miriam-gene:27185, lld:C0036341; a sio:SIO_001121 . } dgn-np:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_provenance { dgn-np:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_assertion dcterms:description "[In the region 1q42-44 (26.8 cM), the marker D1S251, located near the breakpoint of a balanced translocation t (1;11) (q42.1;q14.3) segregated with schizophrenia, and also near the neurodevelopment-related 'Disrupted in Schizophrenia 1' gene, had a maximum NPL score of 1.73 (P=0.03) under the narrow phenotype model and 2.18 (P=0.01) under the broad phenotype model comprised of schizophrenia, schizoaffective disorder, and other nonaffective psychotic disorders as defined by DSM-IV criteria.]. 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:12740602; 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:NP393860.RADX2v_-6aQHSutLD9uJVCARYoPGhSuMUqXgZbkPbKdpk130_publicationInfo { this: dcterms:created "2016-05-13T12:44:43+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" . }