@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY> .
@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:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_head {
  this: np:hasAssertion dgn-np:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_assertion;
    np:hasProvenance dgn-np:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_provenance;
    np:hasPublicationInfo dgn-np:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_assertion a np:Assertion .
  
  dgn-np:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_provenance a np:Provenance .
  
  dgn-np:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_assertion {
  miriam-gene:27185 a ncit:C16612 .
  
  lld:C0041696 a ncit:C7057 .
  
  dgn-gda:DGNf9b8a4589c5cb056e0745170283e3eb5 sio:SIO_000628 miriam-gene:27185, lld:C0041696;
    a sio:SIO_001121 .
}

dgn-np:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_provenance {
  dgn-np:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_assertion dcterms:description
      "[Disrupted in schizophrenia 1 (DISC1) has been associated with risk of schizophrenia, schizoaffective disorder, bipolar disorder, major depression, autism and Asperger syndrome, but apart from in the original translocation family, true causal variants have yet to be confirmed.]. 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:18317464;
    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:NP738202.RARkLROphePn8O04dmnnyx6GO1zAG0AMraRRnIQEnpAkY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:28+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" .
}