@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk> .
@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:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_head {
  this: np:hasAssertion dgn-np:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_assertion ;
    np:hasProvenance dgn-np:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_provenance ;
    np:hasPublicationInfo dgn-np:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_assertion a np:Assertion .
  dgn-np:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_provenance a np:Provenance .
  dgn-np:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_assertion {
  miriam-gene:1063 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
  dgn-gda:DGNca34a2ae33a6adab90a689b357f73a70 sio:SIO_000628 miriam-gene:1063 , lld:C0006142 ;
    a sio:SIO_001122 .
}
dgn-np:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_provenance {
  dgn-np:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_assertion dcterms:description "[As a main observation, carriers of the A allele of the CENPF SNP rs438034 had a worse BC-specific survival compared to the wild type genotype GG carriers (hazard ratio (HR) 2.65, 95% confidence interval (CI) 1.19-5.90), although they were less likely to have regional lymph node metastases (odds ratio (OR) 0.71, 95% CI 0.51-1.01) and tumours of stage II-IV (OR 0.73, 95% CI 0.54-0.99).]. 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:19008095 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP78034.RADsJcNZAHE8coVqBveUwe-BC1lyCY41S9uX47dVVZIFk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:38+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" .
}