@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_head {
  this: np:hasAssertion dgn-np:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_assertion;
    np:hasProvenance dgn-np:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_provenance;
    np:hasPublicationInfo dgn-np:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_assertion a np:Assertion .
  
  dgn-np:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_provenance a np:Provenance .
  
  dgn-np:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_assertion {
  miriam-gene:902 a ncit:C16612 .
  
  lld:C0007131 a ncit:C7057 .
  
  dgn-gda:DGNf978fb55d6e91e7fab70f44336b0e5f8 sio:SIO_000628 miriam-gene:902, lld:C0007131;
    a sio:SIO_001121 .
}

dgn-np:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_provenance {
  dgn-np:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_assertion dcterms:description
      "[54 potentially functional polymorphisms in key cell cycle genes (CDK1, CDK2, CDK4, CDK6, CDK7, CCND1, CCND2, CCND3, CCNE1, CCNA1, CCNA2, CCNB1, CCNH, p15, p16, p18, p19, p21, p27, Cdc25A and Cdc25B) were genotyped by using Illumina SNP genotyping platform to evaluate their associations with survival of NSCLC in a clinical cohort of 568 patients.]. 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:21145615;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP288426.RAm3GOCJXJiz6eKdZxHmH4i36cpbHtz7x-QG2T_gyQTac130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:24+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}