@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U> .
@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:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_head {
  this: np:hasAssertion dgn-np:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_assertion;
    np:hasProvenance dgn-np:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_provenance;
    np:hasPublicationInfo dgn-np:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_assertion a np:Assertion .
  
  dgn-np:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_provenance a np:Provenance .
  
  dgn-np:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_assertion {
  miriam-gene:2903 a ncit:C16612 .
  
  lld:C0005586 a ncit:C7057 .
  
  dgn-gda:DGN3281c2342c25c6ce4520e0470c623150 sio:SIO_000628 miriam-gene:2903, lld:C0005586;
    a sio:SIO_001121 .
}

dgn-np:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_provenance {
  dgn-np:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_assertion dcterms:description
      "[We examined the role of the N-methyl-D-aspartate receptor 2A subunit (GRIN2A) gene on 16p13.3, a region thought to be linked to bipolar disorder, (1) because in a prior study we identified a functional and polymorphic (GT)n repeat in the 5' regulatory region of the gene, with longer alleles showing lower transcriptional activity and an over representation in schizophrenia, and (2) because of the suggestion of a genetic overlap between affective disorder and 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:12809987;
    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:NP930228.RAYT9JAn2cZ95036SM9CFZTCOMAGIL56qqSzHknDkTT9U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:30+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" .
}