@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js> .
@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:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_head {
  this: np:hasAssertion dgn-np:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_assertion;
    np:hasProvenance dgn-np:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_provenance;
    np:hasPublicationInfo dgn-np:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_assertion a np:Assertion .
  
  dgn-np:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_provenance a np:Provenance .
  
  dgn-np:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0009404 a ncit:C7057 .
  
  dgn-gda:DGNc1c016e4dbfc25a3e34ee38c3b461256 sio:SIO_000628 miriam-gene:7157, lld:C0009404;
    a sio:SIO_001121 .
}

dgn-np:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_provenance {
  dgn-np:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_assertion dcterms:description
      "[We evaluated the relationship between p53 mutation and the major form of genomic instability in sporadic colorectal tumors, namely, that involving DNA breakage, which leads to chromosomal translocations, insertions, deletions, and gene amplification.]. 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:8931611;
    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:NP205350.RAtnWR5mLtxuLFq7ECx55uC9P5vLFLqdRx11bXuBO58Js130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:53+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" .
}