@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o> .
@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:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_head {
  this: np:hasAssertion dgn-np:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_assertion;
    np:hasProvenance dgn-np:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_provenance;
    np:hasPublicationInfo dgn-np:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_assertion a np:Assertion .
  
  dgn-np:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_provenance a np:Provenance .
  
  dgn-np:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_assertion {
  miriam-gene:27185 a ncit:C16612 .
  
  lld:C0236792 a ncit:C7057 .
  
  dgn-gda:DGN3b30c065206e2695a386a66dc6066543 sio:SIO_000628 miriam-gene:27185, lld:C0236792;
    a sio:SIO_001121 .
}

dgn-np:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_provenance {
  dgn-np:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_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:NP214570.RAkJBmsTOfFO6FySJnTfAAly4OREkt-2KNXPLipHhBv8o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:59+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}