@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98> .
@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:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_head {
  this: np:hasAssertion dgn-np:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_assertion;
    np:hasProvenance dgn-np:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_provenance;
    np:hasPublicationInfo dgn-np:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_assertion a np:Assertion .
  
  dgn-np:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_provenance a np:Provenance .
  
  dgn-np:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_assertion {
  miriam-gene:64067 a ncit:C16612 .
  
  lld:C0004936 a ncit:C7057 .
  
  dgn-gda:DGN0cb5c8243177d5e9448879763b79d10c sio:SIO_000628 miriam-gene:64067, lld:C0004936;
    a sio:SIO_001122 .
}

dgn-np:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_provenance {
  dgn-np:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_assertion dcterms:description
      "[Findings also revealed evidence suggesting that several genes may have effects that transcend clinical diagnostic boundaries, including variants in NPAS3 that showed pleiotropic effects across schizophrenia, bipolar disorder, and major depressive disorder.]. 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:20713499;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP95392.RAdSpmt4X8MOZ3gFdL9tk6khnp91kVH1bbcAD3Ddo0F98130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:47+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" .
}