@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM> .
@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:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_head {
  this: np:hasAssertion dgn-np:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_assertion;
    np:hasProvenance dgn-np:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_provenance;
    np:hasPublicationInfo dgn-np:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_assertion a np:Assertion .
  
  dgn-np:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_provenance a np:Provenance .
  
  dgn-np:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_assertion {
  miriam-gene:627 a ncit:C16612 .
  
  lld:C2063866 a ncit:C7057 .
  
  dgn-gda:DGN2f76bb77b6ec7847a596d107c21e25a8 sio:SIO_000628 miriam-gene:627, lld:C2063866;
    a sio:SIO_001121 .
}

dgn-np:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_provenance {
  dgn-np:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_assertion dcterms:description
      "[These results suggest that the interactions of BDNF (rs6265) with NTRK2 (rs1387923, rs2769605 and rs1565445) gene polymorphisms likely play an essential role in the development of TRD in Han Chinese MDD patients.]. 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:23137999;
    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:NP330681.RAhvKN-EVT2oexyVq6XNn0eS5ZKSGlrcOJQ_F8DuHbggM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:14+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" .
}