@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE> .
@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:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_head {
  this: np:hasAssertion dgn-np:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_assertion ;
    np:hasProvenance dgn-np:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_provenance ;
    np:hasPublicationInfo dgn-np:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_assertion a np:Assertion .
  dgn-np:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_provenance a np:Provenance .
  dgn-np:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  lld:C1512433 a ncit:C7057 .
  dgn-gda:DGNc6598d9f8f89e8506142deec3e8a64be sio:SIO_000628 miriam-gene:1029 , lld:C1512433 ;
    a sio:SIO_001121 .
}
dgn-np:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_provenance {
  dgn-np:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_assertion dcterms:description "[To allow objective classification, we have exploited the peculiar characteristics of chemiluminescence detection, such as high sensitivity and easy quantification of the luminescence signal, to perform sequentially in the same tissue section both an immunohistochemical quantitative detection of p16(INK4A) (a protein marker of high-grade CIN lesions) and an in situ hybridization for human papillomavirus (generally accepted as a necessary but insufficient cause of cervical carcinoma).]. 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:19263042 ;
    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:NP700672.RAaC_GRK7Y3DqXFS-nUEByUOV4sagYwAVpFN3xbFFaSRE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:06+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" .
}