@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128> .
@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:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_head {
  this: np:hasAssertion dgn-np:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_assertion;
    np:hasProvenance dgn-np:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_provenance;
    np:hasPublicationInfo dgn-np:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_assertion a np:Assertion .
  
  dgn-np:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_provenance a np:Provenance .
  
  dgn-np:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_assertion {
  miriam-gene:10923 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGN7b601ce893528a9e22a6cb2def42121a sio:SIO_000628 miriam-gene:10923, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_provenance {
  dgn-np:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_assertion dcterms:description
      "[Here we report, for the first time in the literature, the high incidences of p16 and p15 alterations in MM, not by homozygous deletions or mutations, but solely by hypermethylation of the 5' CpG islands, which may be a specific mechanism in this disease.]. 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:9116295;
    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:NP482692.RAVUu9ZdT6FlbiosmoUhTgVcaNBRauQY3c1Pxtc7k5128130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:49+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" .
}