@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_head {
  this: np:hasAssertion dgn-np:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_assertion ;
    np:hasProvenance dgn-np:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_provenance ;
    np:hasPublicationInfo dgn-np:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_assertion a np:Assertion .
  dgn-np:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_provenance a np:Provenance .
  dgn-np:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_assertion {
  miriam-gene:6886 a ncit:C16612 .
  lld:C0005684 a ncit:C7057 .
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dgn-np:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_provenance {
  dgn-np:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_assertion dcterms:description "[Validation in an independent sample of 212 BC patients enabled the optimization of five methylation targets, including VAX1, KCNV1, TAL1, PPOX1, and CFTR, which was obtained in our previous study, for BC diagnosis with a sensitivity and specificity of 88.68% and 87.25%, 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:22529986 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP977158.RAFFt09PnGv_dL7sJL8duxz4wq7uEUySTXVahw2G50mlE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:07+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}