@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4> .
@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:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_head {
  this: np:hasAssertion dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_assertion ;
    np:hasProvenance dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_provenance ;
    np:hasPublicationInfo dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_assertion a np:Assertion .
  dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_provenance a np:Provenance .
  dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_assertion {
  miriam-gene:3569 a ncit:C16612 .
  lld:C0020459 a ncit:C7057 .
  dgn-gda:DGNd5f714c3cdf1ac24649573d5c93d9b71 sio:SIO_000628 miriam-gene:3569 , lld:C0020459 ;
    a sio:SIO_001121 .
}
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_provenance {
  dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_assertion dcterms:description "[Subjects homozygous for the C allele at position -174 of the IL-6 gene (SfaNI genotype), associated to lower plasma IL-6 levels, showed significantly lower integrated area under the curve of serum glucose concentrations (AUCglucose) after an oral glucose tolerance test, lower blood glycosylated hemoglobin, lower fasting insulin levels, lower total and differential white blood cell count (a putative marker of peripheral IL-6 action), and an increased insulin sensitivity index than carriers of the G allele, despite similar age and body composition.]. 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:10868978 ;
    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:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:11+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" .
}