@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4> .
@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:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_head {
  this: np:hasAssertion dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_assertion;
    np:hasProvenance dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_provenance;
    np:hasPublicationInfo dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_assertion a np:Assertion .
  
  dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_provenance a np:Provenance .
  
  dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C1961102 a ncit:C7057 .
  
  dgn-gda:DGNd9c30decf1152ee32188d55fb413ce7f sio:SIO_000628 miriam-gene:595, lld:C1961102;
    a sio:SIO_001121 .
}

dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_provenance {
  dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_assertion dcterms:description
      "[To study the association between cyclin D1 (CCND1) polymorphic variants and acute lymphoblastic leukemia (ALL) and breast cancer cases and the possibility of having different (CCND1) polymorphic variants in the development of ALL and breast cancer.]. 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:23613410;
    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:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:23+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" .
}