@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP579783.RAkq8HTjz4jSM72fxKpRahZxk2w9EPqYAbh0NYDYLWO84> .
@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#> .
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  this: np:hasAssertion dgn-np:NP579783.RAkq8HTjz4jSM72fxKpRahZxk2w9EPqYAbh0NYDYLWO84130_assertion ;
    np:hasProvenance dgn-np:NP579783.RAkq8HTjz4jSM72fxKpRahZxk2w9EPqYAbh0NYDYLWO84130_provenance ;
    np:hasPublicationInfo dgn-np:NP579783.RAkq8HTjz4jSM72fxKpRahZxk2w9EPqYAbh0NYDYLWO84130_publicationInfo ;
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}
dgn-np:NP579783.RAkq8HTjz4jSM72fxKpRahZxk2w9EPqYAbh0NYDYLWO84130_assertion {
  miriam-gene:6638 a ncit:C16612 .
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    a sio:SIO_001121 .
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dgn-np:NP579783.RAkq8HTjz4jSM72fxKpRahZxk2w9EPqYAbh0NYDYLWO84130_provenance {
  dgn-np:NP579783.RAkq8HTjz4jSM72fxKpRahZxk2w9EPqYAbh0NYDYLWO84130_assertion dcterms:description "[We demonstrated that: (i) the aberrant epigenetic profile, as delineated by the cancer status, is a reversible modification, evidenced by our ability to restore the normal patterns of replication in three unrelated loci (CEN15, SNRPN and RB1) by introducing an archetypical demethylating agent, 5-azacytidine; (ii) following the rehabilitating effect of demethylation, an imprinted gene (SNRPN) retains its original parental imprint; and (iii) the choice of an allele between early or late replication in the aberrant asynchronous replication, delineated by the cancer status, is not random but is independent of the parental origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP579783.RAkq8HTjz4jSM72fxKpRahZxk2w9EPqYAbh0NYDYLWO84130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:49+02:00"^^xsd:dateTime ;
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    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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