@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4> .
@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:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_head {
  this: np:hasAssertion dgn-np:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_assertion;
    np:hasProvenance dgn-np:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_provenance;
    np:hasPublicationInfo dgn-np:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_assertion a np:Assertion .
  
  dgn-np:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_provenance a np:Provenance .
  
  dgn-np:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNa52471501878de1e4e5284bc466ce446 sio:SIO_000628 miriam-gene:5624, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_provenance {
  dgn-np:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_assertion dcterms:description
      "[The underlying propensity for mutation at the APC gene is intriguing, while the greater frequency of mutation in cells defective for DNA repair has relevance to understanding events leading to colorectal cancer and other malignancies.]. 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:22294772;
    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:NP647904.RAFBWezcfMzYt7dCuFK7ig1i6rHnJI76oOTh6hMaTpwW4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:09+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" .
}