@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg> .
@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:NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg130_head {
  this: np:hasAssertion dgn-np:NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg130_assertion ;
    np:hasProvenance dgn-np:NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg130_provenance ;
    np:hasPublicationInfo dgn-np:NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg130_provenance a np:Provenance .
  dgn-np:NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg130_assertion {
  miriam-gene:5027 a ncit:C16612 .
  lld:C0005586 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg130_provenance {
  dgn-np:NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg130_assertion dcterms:description "[Although genetic findings were not always consistently replicated, several studies demonstrated that single nucleotide polymorphisms (SNPs) in the human P2X7 gene (P2RX7) show significant association with major depressive disorder and bipolar 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:23269209 ;
    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:NP810089.RA8cmBininBxTLB9Ruyzk5MihgfPo7pFWqxtlQluldZqg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:16+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 ;
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}