@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk> .
@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:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_head {
  this: np:hasAssertion dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_assertion ;
    np:hasProvenance dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_provenance ;
    np:hasPublicationInfo dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_assertion a np:Assertion .
  dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_provenance a np:Provenance .
  dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_assertion {
  miriam-gene:595 a ncit:C16612 .
  lld:C1947901 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_provenance {
  dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_assertion dcterms:description "[It is of interest to evaluate concurrently the alterations of both genes on the same series of NSCLCs, to investigate whether cyclin D1 and RB alterations are alternative pathways leading to inactivation of the G1 restriction point or if they can occur in the same tumor, possibly exerting an additive effect on cancer progression.]. 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:9462706 ;
    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:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:21+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}