@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g> .
@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:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_head {
  this: np:hasAssertion dgn-np:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_assertion;
    np:hasProvenance dgn-np:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_provenance;
    np:hasPublicationInfo dgn-np:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_assertion a np:Assertion .
  
  dgn-np:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_provenance a np:Provenance .
  
  dgn-np:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0001815 a ncit:C7057 .
  
  dgn-gda:DGN2c3f4725e4bb5d481664d2eb64880ac7 sio:SIO_000628 miriam-gene:1029, lld:C0001815;
    a sio:SIO_001121 .
}

dgn-np:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_provenance {
  dgn-np:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_assertion dcterms:description
      "[Using polymerase chain reaction-based methylation analysis assay methods, with substantiation using Southern blot analysis, the study showed no hypermethylation of p15 or p16 genes in the chronic phase of AMM, but p15 gene hypermethylation was found in four patients (40%) and p16 gene hypermethylation in two patients (20%) when they were in leukaemic transformation stage.]. 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:11849214;
    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:NP513423.RAfdLRgvkDd5De4nGqEmQOsHX2nTVs6NMsHCWkVLLt21g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:06+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" .
}