@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg> .
@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:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_head {
  this: np:hasAssertion dgn-np:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_assertion;
    np:hasProvenance dgn-np:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_provenance;
    np:hasPublicationInfo dgn-np:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_assertion a np:Assertion .
  
  dgn-np:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_provenance a np:Provenance .
  
  dgn-np:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_assertion {
  miriam-gene:79068 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGN30917772d78dcbdcbdc89a8957aa5cdc sio:SIO_000628 miriam-gene:79068, lld:C0524620;
    a sio:SIO_001121 .
}

dgn-np:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_provenance {
  dgn-np:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_assertion dcterms:description
      "[The C allele of the rs7204609 polymorphism in the FTO gene increased the chance for the presence of MetS, especially central obesity, and microalbuminuria, independently of energy and nutrient intakes in this sample of type 2 diabetic patients from Southern Brazil.]. 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:21741858;
    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:NP258890.RA_ZdzCdbjKGUQBokjI-i0yntpjc_MO_ljABVJf74Qqeg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}