@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE> .
@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:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_head {
  this: np:hasAssertion dgn-np:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_assertion ;
    np:hasProvenance dgn-np:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_provenance ;
    np:hasPublicationInfo dgn-np:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_assertion a np:Assertion .
  dgn-np:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_provenance a np:Provenance .
  dgn-np:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  lld:C0022665 a ncit:C7057 .
  dgn-gda:DGN5c5ccaef5864da4412ee5e372daded53 sio:SIO_000628 miriam-gene:1029 , lld:C0022665 ;
    a sio:SIO_001121 .
}
dgn-np:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_provenance {
  dgn-np:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_assertion dcterms:description "[However, neither p15INK4B nor p16INK4 were deleted in 12 of 12 primary kidney tumors examined, suggesting that deletion of these genes is not directly involved in the process of renal tumor development but may be related to tumor progression or autonomous growth 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:7712460 ;
    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:NP799166.RAGDSSHFapLdRxdMyOjtRqyOrqO0P6VcP99v-FmqWqyfE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:10+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" .
}