@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4> .
@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:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_head {
  this: np:hasAssertion dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_assertion;
    np:hasProvenance dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_provenance;
    np:hasPublicationInfo dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_assertion a np:Assertion .
  
  dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_provenance a np:Provenance .
  
  dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_assertion {
  miriam-gene:4170 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN05a7deb510a2c506283e1224aec74119 sio:SIO_000628 miriam-gene:4170, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_provenance {
  dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_assertion dcterms:description
      "[A common insertional polymorphism in promoter of MCL1, a member of BCL2 family gene with the dual regulatory functions, has been shown to be functional in leukemia, but its association with cancer predisposition and prognosis has not been well established.]. 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:21887682;
    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:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}