@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o> .
@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:NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o130_head {
   this: np:hasAssertion dgn-np:NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o130_assertion ;
    np:hasProvenance dgn-np:NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o130_provenance ;
    np:hasPublicationInfo dgn-np:NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o130_provenance a np:Provenance .
  dgn-np:NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o130_assertion {
   miriam-gene:1543 a ncit:C16612 .
  lld:C0302592 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o130_provenance {
   dgn-np:NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o130_assertion dcterms:description "[Meta-analysis of the ten studies on cervical cancer suggested a significant association between the CYP1A1 T3801C polymorphism and cervical cancer risk (C vs. T, OR 1.38, 95 % CI 1.05-1.82, P = 0.02; CC vs. TT, OR 2.06, 95 % CI 1.15-3.70, P = 0.02; CC/CT vs. TT, OR 1.45, 95 % CI 1.03-2.02, P = 0.03; CC vs. TT/CT, OR 1.56, 95 % CI 1.20-2.03, P < 0.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP776756.RAXuNCjyKM-LOvBVzfEPaR2ZOBdXXhWZCPqdbmx102x5o130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:50+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 ;
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}