@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0> .
@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:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_head {
  this: np:hasAssertion dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_assertion;
    np:hasProvenance dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_provenance;
    np:hasPublicationInfo dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_assertion a np:Assertion .
  
  dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_provenance a np:Provenance .
  
  dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_assertion {
  miriam-gene:5578 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN1212f1815ed878bab99132c466f0ae7e sio:SIO_000628 miriam-gene:5578, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_provenance {
  dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_assertion dcterms:description
      "[Three polymorphisms (GRIN2B rs220599, GRM3 rs2189814 and PRKCA rs8074995) were associated with episodic verbal memory in both control and patients with cognitive deficit, but not in cognitively spared patients or the pooled schizophrenia sample.]. 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:21281445;
    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:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:29+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" .
}