@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM> .
@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:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_head {
   this: np:hasAssertion dgn-np:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_assertion ;
    np:hasProvenance dgn-np:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_provenance ;
    np:hasPublicationInfo dgn-np:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_assertion a np:Assertion .
  dgn-np:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_provenance a np:Provenance .
  dgn-np:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_assertion {
   miriam-gene:80351 a ncit:C16612 .
  lld:C0011860 a ncit:C7057 .
  dgn-gda:DGN0ae7451258d17ca0ab638317d42f9427 sio:SIO_000628 miriam-gene:80351 , lld:C0011860 ;
    a sio:SIO_001121 .
}
dgn-np:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_provenance {
   dgn-np:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_assertion dcterms:description "[The association between 150 tagging-SNPs (tSNPs) of 11 telomere-pathway genes (TERC, UCP1, TERT, POT1, TNKS, TERF1, TNKS2, TEP1, ACD, TERF2 and TERF2IP) and incident T2D was investigated in 22,715 Caucasian female participants of the prospective Women's Genome Health 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:21665207 ;
    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:NP502148.RABFv_o6HBNFHcLZAPetirGrQUvLGR7OIDXxHXqFJJJFM130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:59+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> ;
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}