@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs> .
@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:NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_head {
   this: np:hasAssertion dgn-np:NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_assertion ;
    np:hasProvenance dgn-np:NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_provenance ;
    np:hasPublicationInfo dgn-np:NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_assertion a np:Assertion .
  dgn-np:NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_provenance a np:Provenance .
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}
dgn-np:NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_assertion {
   miriam-gene:896 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
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    a sio:SIO_001122 .
}
dgn-np:NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_provenance {
   dgn-np:NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_assertion dcterms:description "[We examined associations between common germline genetic variation in 13 genes involved in cell cycle control (CCND1, CCND2, CCND3, CCNE1, CDK2 p33, CDK4, CDK6, CDKN1A p21, Cip1, CDKN1B p27, Kip1, CDKN2A p16, CDKN2B p15, CDKN2C p18, and CDKN2D p19) and survival among women diagnosed with invasive breast cancer participating in the SEARCH (Studies of Epidemiology and Risk factors in Cancer Heredity) breast cancer study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP78970.RAoEfv844rvgd13nsDegdroSt5LAO-OIXuiZ20UUBTiPs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}