@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A> .
@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:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_head {
  this: np:hasAssertion dgn-np:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_assertion;
    np:hasProvenance dgn-np:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_provenance;
    np:hasPublicationInfo dgn-np:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_assertion a np:Assertion .
  
  dgn-np:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_provenance a np:Provenance .
  
  dgn-np:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_assertion {
  miriam-gene:79068 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN5ebc67442d81bd19bc42badfca37fcc8 sio:SIO_000628 miriam-gene:79068, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_provenance {
  dgn-np:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_assertion dcterms:description
      "[The aim of this study was to clarify the role of single nucleotide polymorphisms (SNPs) in FTO in metabolic disorders such as hypertension, obesity, diabetes, dyslipidemia, insulin resistance and metabolic syndrome in the Japanese general population using data from a cohort study in Hokkaido, namely the Tanno-Sobetsu study.]. 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:20075932;
    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:NP609809.RAY5eMdAK7REMHKiLJ1ycNJ_QOj0nVgN7zB-2hddUTl7A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:06+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" .
}