@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_head {
  this: np:hasAssertion dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion ;
    np:hasProvenance dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance ;
    np:hasPublicationInfo dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion a np:Assertion .
  dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance a np:Provenance .
  dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion {
  miriam-gene:27184 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
  dgn-gda:DGN306be339a32f566bf614c43258c4406b sio:SIO_000628 miriam-gene:27184 , lld:C0036341 ;
    a sio:SIO_001121 .
}
dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_provenance {
  dgn-np:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_assertion dcterms:description "[The results of karyotypic, clinical, and ERP investigations of this family suggest that the recently described genes DISC1 and DISC2, which are directly disrupted by the breakpoint on chromosome 1, may have a role in the development of a disease phenotype that includes schizophrenia as well as unipolar and bipolar affective disorders.]. 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:11443544 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP569986.RAvt9lhFivcBJWtoZyPkKPEo70WMTm7-PpnhdpjnVi8rA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:43+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}