@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs> .
@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:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_head {
  this: np:hasAssertion dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_assertion ;
    np:hasProvenance dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_provenance ;
    np:hasPublicationInfo dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_assertion a np:Assertion .
  dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_provenance a np:Provenance .
  dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_assertion {
  miriam-gene:3021 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN98f2e4e352a5f53cd14d9cb1eeac7523 sio:SIO_000628 miriam-gene:3021 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_provenance {
  dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_assertion dcterms:description "[Recently, mutations in the ATRX/DAXX chromatin remodeling complex and histone H3.3 were found to correlate with features of ALT in pancreatic neuroendocrine cancers, pediatric glioblastomas, and other tumors of the central nervous system, suggesting that these mutations might contribute to the activation of the ALT pathway in these 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:22829774 ;
    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:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:35+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" .
}