@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8> .
@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:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_head {
  this: np:hasAssertion dgn-np:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_assertion;
    np:hasProvenance dgn-np:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_provenance;
    np:hasPublicationInfo dgn-np:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_assertion a np:Assertion .
  
  dgn-np:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_provenance a np:Provenance .
  
  dgn-np:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_assertion {
  miriam-gene:4852 a ncit:C16612 .
  
  lld:C0085762 a ncit:C7057 .
  
  dgn-gda:DGNb210673f15cb042be0ee85c0373a8fd4 sio:SIO_000628 miriam-gene:4852, lld:C0085762;
    a sio:SIO_001122 .
}

dgn-np:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_provenance {
  dgn-np:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_assertion dcterms:description
      "[The 1128C allele was observed in all populations of European descent and the Israeli population, with a mean frequency of about 4%. The allele frequency showed a geographical north to south gradient of decreasing frequency. The highest allele frequencies were found in Nordic countries. The NPY 1128C allele might originate in the north of Europe, and then spread to neighboring regions.]. 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:14628185;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP53716.RADrZd0Lms2y-Sx_aYSSxfdFIguXG5kKeupM7CrVY3kj8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}