@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM> .
@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:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_head {
  this: np:hasAssertion dgn-np:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_assertion;
    np:hasProvenance dgn-np:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_provenance;
    np:hasPublicationInfo dgn-np:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_assertion a np:Assertion .
  
  dgn-np:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_provenance a np:Provenance .
  
  dgn-np:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_assertion {
  miriam-gene:4160 a ncit:C16612 .
  
  lld:C0006370 a ncit:C7057 .
  
  dgn-gda:DGNb037fc755dbc4007ccc5fa364b800c88 sio:SIO_000628 miriam-gene:4160, lld:C0006370;
    a sio:SIO_001121 .
}

dgn-np:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_provenance {
  dgn-np:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_assertion dcterms:description
      "[Melanocortin-4 receptor gene (MC4R) variants are associated with obesity and binge eating disorder (BED), whereas the more prevalent proopiomelanocortin (POMC) and leptin receptor gene (LEPR) mutations are rarely associated with obesity or BED.]. 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:15585384;
    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:NP788697.RANAvLRjtzJS1v_JFx17evzOZI_I8DIP1t_WDdQGC4NjM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:01+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" .
}