@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g> .
@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:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_head {
  this: np:hasAssertion dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_assertion;
    np:hasProvenance dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_provenance;
    np:hasPublicationInfo dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_assertion a np:Assertion .
  
  dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_provenance a np:Provenance .
  
  dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_assertion {
  miriam-gene:572 a ncit:C16612 .
  
  lld:C0001418 a ncit:C7057 .
  
  dgn-gda:DGN4f9ec9e812ac081040a708abfae20211 sio:SIO_000628 miriam-gene:572, lld:C0001418;
    a sio:SIO_001121 .
}

dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_provenance {
  dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_assertion dcterms:description
      "[To explore the possibility that the genetic alterations of Bad might be involved in the development of human cancers, we analyzed the entire coding region and all splice sites of human Bad gene in 47 colon adenocarcinomas.]. 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:15033904;
    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:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:07+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" .
}