@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70> .
@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:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_head {
  this: np:hasAssertion dgn-np:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_assertion;
    np:hasProvenance dgn-np:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_provenance;
    np:hasPublicationInfo dgn-np:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_assertion a np:Assertion .
  
  dgn-np:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_provenance a np:Provenance .
  
  dgn-np:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_assertion {
  miriam-gene:3552 a ncit:C16612 .
  
  lld:C0595905 a ncit:C7057 .
  
  dgn-gda:DGN31ea3374e0734c1f8dce2e7d06bc0185 sio:SIO_000628 miriam-gene:3552, lld:C0595905;
    a sio:SIO_001121 .
}

dgn-np:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_provenance {
  dgn-np:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_assertion dcterms:description
      "[Interleukin-1 (IL-1) cluster (chromosome 2q13) genetic variability, previously associated with an increased risk both for schizophrenia and for bipolar disorder, has been also associated with gray matter (GM) deficits, ventricular enlargement and hypoactivity of prefrontal cortex in schizophrenia.]. 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:19125864;
    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:NP655976.RAnj3g5vhXjSCUOlVoEFCV3n2zTy6ZaT-v7SyPk190c70130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:35+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" .
}