@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw> .
@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:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_head {
  this: np:hasAssertion dgn-np:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_assertion ;
    np:hasProvenance dgn-np:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_provenance ;
    np:hasPublicationInfo dgn-np:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_assertion a np:Assertion .
  dgn-np:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_provenance a np:Provenance .
  dgn-np:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_assertion {
  miriam-gene:2837 a ncit:C16612 .
  lld:C0242379 a ncit:C7057 .
  dgn-gda:DGNa2296e5627b656234f790b620082e4de sio:SIO_000628 miriam-gene:2837 , lld:C0242379 ;
    a sio:SIO_001121 .
}
dgn-np:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_provenance {
  dgn-np:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_assertion dcterms:description "[First, we genotyped seven SNPs in a Chinese Han population with 600 lung cancer patients and 600 matched healthy controls and found that compared with the TT genotype of rs2239680 in 3' UTR of baculoviral IAP repeat containing 5 (BIRC5), C allele was associated with a significantly increased risk of lung cancer and advanced pathologic stage, with the odds ratio for participants carrying the CT or CC genotype being 1.50 [95% confidence interval (CI) 1.20-1.89, P<0.01] and 2.29 (95% CI 1.64-3.18, P<0.01), respectively.]. 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:23232114 ;
    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:NP448768.RA80SkD5ulTb0wj8j0WfIihyJuJSpwPo4zoUNIAlVOXvw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:27+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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    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}