@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY> .
@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:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_head {
  this: np:hasAssertion dgn-np:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_assertion ;
    np:hasProvenance dgn-np:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_provenance ;
    np:hasPublicationInfo dgn-np:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_assertion a np:Assertion .
  dgn-np:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_provenance a np:Provenance .
  dgn-np:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_assertion {
  miriam-gene:7015 a ncit:C16612 .
  lld:C0376358 a ncit:C7057 .
  dgn-gda:DGN8ec765973e9a8fdd351ab06399be27e0 sio:SIO_000628 miriam-gene:7015 , lld:C0376358 ;
    a sio:SIO_001122 .
}
dgn-np:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_provenance {
  dgn-np:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_assertion dcterms:description "[This is the first study to report that rare hTERT VNTRs are associated with prostate cancer predisposition and that the VNTRs can induce enhanced levels of hTERT promoter activity in prostate cancer cell lines. Thus, the hTERT-VNTR2-2nd locus may function as a modifier of prostate cancer risk by affecting gene expression.]. 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:20659312 ;
    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:NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:45+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> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}