@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0> .
@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:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_head {
  this: np:hasAssertion dgn-np:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_assertion;
    np:hasProvenance dgn-np:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_provenance;
    np:hasPublicationInfo dgn-np:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_assertion a np:Assertion .
  
  dgn-np:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_provenance a np:Provenance .
  
  dgn-np:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_assertion {
  miriam-gene:2904 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGN72c298241c206812fcad237158588f3e sio:SIO_000628 miriam-gene:2904, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_provenance {
  dgn-np:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_assertion dcterms:description
      "[In the perirhinal cortex we detected decreased expression of GluR5 in all three diagnoses, of GluR1, GluR3, NR2B in both BD and MDD, and decreased NR1 and NR2A in BD and MDD, respectively.]. 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:17299517;
    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:NP485199.RACOua3N9j2uCni4eFF0rIEvectm-B6zPV_7oNUmnOJS0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:50+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" .
}