@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M> .
@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:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_head {
  this: np:hasAssertion dgn-np:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_assertion;
    np:hasProvenance dgn-np:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_provenance;
    np:hasPublicationInfo dgn-np:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_assertion a np:Assertion .
  
  dgn-np:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_provenance a np:Provenance .
  
  dgn-np:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_assertion {
  miriam-gene:5225 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_provenance {
  dgn-np:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_assertion dcterms:description
      "[Polygenic scores based on family study results were used to predict case-control status in the Schizophrenia Psychiatric GWAS Consortium (PGC) data set, and consistency of direction of effect with the family study was determined for top SNPs in the PGC GWAS analysis.]. 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:22885689;
    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:NP655591.RA_WzTIwu3KQ6AK0cGLdzDFP4jCOxlZr6Hi3SPI33j88M130_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>,
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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" .
}