@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I> .
@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:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_head {
  this: np:hasAssertion dgn-np:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_assertion;
    np:hasProvenance dgn-np:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_provenance;
    np:hasPublicationInfo dgn-np:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_assertion a np:Assertion .
  
  dgn-np:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_provenance a np:Provenance .
  
  dgn-np:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_assertion {
  miriam-gene:8170 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN596578cb1dc538272a97848dd9c9aada sio:SIO_000628 miriam-gene:8170, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_provenance {
  dgn-np:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_assertion dcterms:description
      "[In order to find the causal variants of NRGN gene in schizophrenia, we searched for genetic variants in the promoter region and all the exons (including both UTR ends and rs12807809) using direct sequencing in a sample of patients with schizophrenia (n=346) and non-psychotic controls (n=345), both being Han Chinese from Taiwan, and conducted an association and functional study.]. 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:22306195;
    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:NP531148.RAgLz7iZIs2qCmDm8PlvtqZID_1B4-5pN7vH3Ug125u4I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+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" .
}