@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI> .
@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:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_head {
  this: np:hasAssertion dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_assertion;
    np:hasProvenance dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_provenance;
    np:hasPublicationInfo dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_assertion a np:Assertion .
  
  dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_provenance a np:Provenance .
  
  dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C1269683 a ncit:C7057 .
  
  dgn-gda:DGN571a6c53cd09feaba3fd494f5b005546 sio:SIO_000628 miriam-gene:1956, lld:C1269683;
    a sio:SIO_001121 .
}

dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_provenance {
  dgn-np:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_assertion dcterms:description
      "[EGFR mutations were associated with lower depression severity and lower rates of probable major depressive disorder in patients with metastatic NSCLC, based on mood screening performed before results of genotyping were known.]. 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:21807767;
    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:NP298895.RAcZpR95_rgReWtg14Jb-YtWmIbP1udCbOY-174bGrqyI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:49+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" .
}