@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg> .
@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:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_head {
  this: np:hasAssertion dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_assertion;
    np:hasProvenance dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_provenance;
    np:hasPublicationInfo dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_assertion a np:Assertion .
  
  dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_provenance a np:Provenance .
  
  dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_assertion {
  miriam-gene:29107 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN131aa4ae14df3f8a6f0e76fc26d36d0f sio:SIO_000628 miriam-gene:29107, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_provenance {
  dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_assertion dcterms:description
      "[Several genes and gene pathways disrupted by aberrant CpG island methylation have now been identified in haematological malignancies, the most frequently studied being the cell cycle inhibitors p16 (now termed CDKN2A; mostly methylated in lymphoid malignancy) and p15 (now termed CDKN2B; commonly methylated in lymphoid and myeloid malignancies).]. 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:17489980;
    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:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:04+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" .
}