@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw> .
@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:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_head {
  this: np:hasAssertion dgn-np:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_assertion;
    np:hasProvenance dgn-np:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_provenance;
    np:hasPublicationInfo dgn-np:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_assertion a np:Assertion .
  
  dgn-np:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_provenance a np:Provenance .
  
  dgn-np:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_assertion {
  miriam-gene:627 a ncit:C16612 .
  
  lld:C0086132 a ncit:C7057 .
  
  dgn-gda:DGN578a644b77abd3c5591fc8353cd8c2bc sio:SIO_000628 miriam-gene:627, lld:C0086132;
    a sio:SIO_001121 .
}

dgn-np:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_provenance {
  dgn-np:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_assertion dcterms:description
      "[The low activity variants of the 5-HTT-linked polymorphic region in the serotonin transporter gene and the Met-allele of a single nucleotide polymorphism (Val66Met) in the gene encoding brain derived neurotrophic factor were independently associated with the presence of stressful life events prior to onset of depression, also when corrected for the effect of age, gender, marital status, personality disorder, neuroticism, and severity of depressive symptoms at the time of interview.]. 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:19339052;
    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:NP393591.RAR4CAa-jeocH65vrIOz89quT9slWW50SsXcvtk70vIKw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:54+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" .
}