@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo> .
@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:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_head {
  this: np:hasAssertion dgn-np:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_assertion;
    np:hasProvenance dgn-np:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_provenance;
    np:hasPublicationInfo dgn-np:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_assertion a np:Assertion .
  
  dgn-np:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_provenance a np:Provenance .
  
  dgn-np:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_assertion {
  miriam-gene:32 a ncit:C16612 .
  
  lld:C0028756 a ncit:C7057 .
  
  dgn-gda:DGNaa979d5467142051f448549ad24d6351 sio:SIO_000628 miriam-gene:32, lld:C0028756;
    a sio:SIO_001121 .
}

dgn-np:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_provenance {
  dgn-np:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_assertion dcterms:description
      "[Twenty five tagging single nucleotide polymorphisms (SNPs) capturing common variants of the ACACB gene were selected and analyzed in two cohorts including 1695 postmenopausal women of the general population and in 161 women with severe obesity (BMI>35).]. 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:21908218;
    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:NP912606.RArAE6FXxptIuSJsRGzXPTa3Y9-LFEaTJSwLNhKmm1guo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:20+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" .
}