@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY> .
@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:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_head {
  this: np:hasAssertion dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_assertion;
    np:hasProvenance dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_provenance;
    np:hasPublicationInfo dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_assertion a np:Assertion .
  
  dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_provenance a np:Provenance .
  
  dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_assertion {
  miriam-gene:627 a ncit:C16612 .
  
  lld:C0085281 a ncit:C7057 .
  
  dgn-gda:DGN8a07dffdaad4f9c379aaf72909e773f7 sio:SIO_000628 miriam-gene:627, lld:C0085281;
    a sio:SIO_001121 .
}

dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_provenance {
  dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_assertion dcterms:description
      "[Potential roles for variants in the human BDNF gene in human brain disorders are supported by findings that include: (a) influences that this trophic factor can exert on important neurons, brain regions, and neurotransmitter systems, (b) changes in BDNF expression that follow altered neuronal activity and drug treatments, and (c) linkages or associations between genetic markers in or near BDNF and human traits and disorders that include depression, schizophrenia, addictions, and Parkinson's disease.]. 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:15666411;
    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:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:34+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" .
}