@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs> .
@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:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_head {
  this: np:hasAssertion dgn-np:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_assertion;
    np:hasProvenance dgn-np:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_provenance;
    np:hasPublicationInfo dgn-np:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_assertion a np:Assertion .
  
  dgn-np:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_provenance a np:Provenance .
  
  dgn-np:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_assertion {
  miriam-gene:6638 a ncit:C16612 .
  
  lld:C0205851 a ncit:C7057 .
  
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dgn-np:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_provenance {
  dgn-np:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_assertion dcterms:description
      "[We analyzed the methylation status of the H19 and SNRPN differential methylated regions (DMRs) and the promoter region of 17 TSGs, and the expression status of H19, IGF2 and SNRPN in 45 GCTs, and found that 25 and 20 were in the normal and abnormal reprogramming pathways, respectively, defined on the basis of the methylation status of the two DMRs and the anatomical tumor site.]. 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:19245437;
    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:NP731983.RAlfbtauYMSjL1dNhAlKIXRZYiCIsPXOzhWWfSh5QaCTs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:24+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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