@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_head {
  this: np:hasAssertion dgn-np:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_assertion;
    np:hasProvenance dgn-np:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_provenance;
    np:hasPublicationInfo dgn-np:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_assertion a np:Assertion .
  
  dgn-np:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_provenance a np:Provenance .
  
  dgn-np:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_assertion {
  miriam-gene:627 a ncit:C16612 .
  
  lld:C0525045 a ncit:C7057 .
  
  dgn-gda:DGN826200a7b4c92a37b2fa4f81eb420c3a sio:SIO_000628 miriam-gene:627, lld:C0525045;
    a sio:SIO_001122 .
}

dgn-np:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_provenance {
  dgn-np:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_assertion dcterms:description
      "[Individuals with schizoaffective disorder and other affective disorders were significantly more likely to carry two copies of the most common BDNF haplotype (containing the valine allele of the Val66Met polymorphism) compared with healthy volunteers.]. 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:19336781;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP729720.RA6ee0NPtbnyWRbqpbM34WLOudyN5Lw0_-qqWxgVBnumw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:16+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}