@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY> .
@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/v3.0.0/void/> .

dgn-np:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_head {
  this: np:hasAssertion dgn-np:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_assertion;
    np:hasProvenance dgn-np:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_provenance;
    np:hasPublicationInfo dgn-np:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_assertion a np:Assertion .
  
  dgn-np:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_provenance a np:Provenance .
  
  dgn-np:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_assertion {
  miriam-gene:627 a ncit:C16612 .
  
  lld:C0020505 a ncit:C7057 .
  
  dgn-gda:DGN289b2cc43b74466b9c5334ef5df90c6a sio:SIO_000628 miriam-gene:627, lld:C0020505;
    a sio:SIO_001122 .
}

dgn-np:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_provenance {
  dgn-np:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_assertion dcterms:description
      "[The existence of mutations that cause haploinsufficiency of BDNF as well as some genetic variants, notably the BDNF p.Val66Met polymorphism, are also associated with the development of obese phenotypes and hyperphagia.]. 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:21945389;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP266420.RAA0-AU6pg4mNqVxZZOzaIQH8jJrfFhkkM7kjQk6r7OGY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:11+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}