@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4> .
@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:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_head {
  this: np:hasAssertion dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_assertion;
    np:hasProvenance dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_provenance;
    np:hasPublicationInfo dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_assertion a np:Assertion .
  
  dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_provenance a np:Provenance .
  
  dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_assertion {
  miriam-gene:79068 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGN47eff6c2fc1fd20c34e3752b9df04549 sio:SIO_000628 miriam-gene:79068, lld:C0524620;
    a sio:SIO_001122 .
}

dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_provenance {
  dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_assertion dcterms:description
      "[Our findings suggest that genes from lipid metabolism pathways have the key role in the genetic background of MetS. We found little evidence for pleiotropy linking dyslipidemia and obesity to the other MetS component traits, such as hypertension and glucose intolerance.]. 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:22399527;
    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:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:35+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" .
}