@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4> .
@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:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_head {
  this: np:hasAssertion dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_assertion ;
    np:hasProvenance dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_provenance ;
    np:hasPublicationInfo dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_assertion a np:Assertion .
  dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_provenance a np:Provenance .
  dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_assertion {
  miriam-gene:51639 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN2c648059ab9148d82437605e65350c77 sio:SIO_000628 miriam-gene:51639 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_provenance {
  dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_assertion dcterms:description "[Thus, these data support a new model in which overcoming senescence plays a critical role in human cancer pathogenesis and requires at least two genetic changes that occur in several combinations that can include either p16 or pRb loss and at least one additional alteration, such as +20q11-q12, -3p13-p14, or -8p21-pter.]. 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:9436977 ;
    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:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:58+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" .
}