@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg> .
@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:NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg130_head {
  this: np:hasAssertion dgn-np:NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg130_assertion ;
    np:hasProvenance dgn-np:NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg130_provenance ;
    np:hasPublicationInfo dgn-np:NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg130_provenance a np:Provenance .
  dgn-np:NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg130_assertion {
  miriam-gene:8739 a ncit:C16612 .
  lld:C0376358 a ncit:C7057 .
  dgn-gda:DGN6f09816ecfcb15687c8acd11648a0047 sio:SIO_000628 miriam-gene:8739 , lld:C0376358 ;
    a sio:SIO_001121 .
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dgn-np:NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg130_provenance {
  dgn-np:NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg130_assertion dcterms:description "[We chose to analyze the hypermethylation status of HRK, the expression of HRK protein and mRNA with 12q13.1 loss of heterozygosity (LOH) and with p53 mutation, and lesion apoptotic indices as determined by transferase-mediated digoxigenin-tagged 16-desoxy-uridine-triphosphate nick end-labeling (TUNEL) assays in 53 prostate cancers.]. 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:18008329 ;
    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:NP671948.RAoyJWU9D-3F4FynAtmVOZw9gKcxRXi_E9akc8Qvcmdzg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:45+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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}