@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I> .
@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 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:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_head {
  this: np:hasAssertion dgn-np:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_assertion;
    np:hasProvenance dgn-np:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_provenance;
    np:hasPublicationInfo dgn-np:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_assertion a np:Assertion .
  
  dgn-np:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_provenance a np:Provenance .
  
  dgn-np:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C0740457 a ncit:C7057 .
  
  dgn-gda:DGNaf1c8f6a86ec6cc91e6d1c6cc161c9f8 sio:SIO_000628 miriam-gene:595, lld:C0740457;
    a sio:SIO_001122 .
}

dgn-np:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_provenance {
  dgn-np:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_assertion dct:description
      "[: These data suggest that the CCND1 variant A allele may be a genetic susceptibility factor with a recessive or gene dose effect for the onset of sporadic RCC. More extensive and larger studies are required to clarify whether the CCND1 genotype is more specifically involved in the onset of a histological subset of RCC or RCC at a younger age.]. 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:15538282;
    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:NP47315.RAmzQyj4u3FU1Ri5vYie2IgHIifdYNdjaHPT4r_aiyM1I130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}