@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA> .
@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:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_head {
  this: np:hasAssertion dgn-np:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_assertion;
    np:hasProvenance dgn-np:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_provenance;
    np:hasPublicationInfo dgn-np:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_assertion a np:Assertion .
  
  dgn-np:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_provenance a np:Provenance .
  
  dgn-np:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_assertion {
  miriam-gene:5111 a ncit:C16612 .
  
  lld:C1512419 a ncit:C7057 .
  
  dgn-gda:DGN0f2f6e55c7e819bcb54e48e15f30c824 sio:SIO_000628 miriam-gene:5111, lld:C1512419;
    a sio:SIO_001121 .
}

dgn-np:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_provenance {
  dgn-np:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_assertion dcterms:description
      "[Recently, the cyclin D-dependent kinase inhibitors (CDKIs) p16INK4a and p15INK4b have been localized within chromosome 9p21, and the presence of p16INK4a point mutations has been demonstrated in familial melanoma and melanoma cell lines in vitro.]. 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:9536218;
    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:NP667508.RAPBO4jW1xLLCXDXCue-A9BenX2GkPQlGOTcIgk-ZLgAA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:43+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" .
}