@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o> .
@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:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_head {
  this: np:hasAssertion dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_assertion;
    np:hasProvenance dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_provenance;
    np:hasPublicationInfo dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_assertion a np:Assertion .
  
  dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_provenance a np:Provenance .
  
  dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0006413 a ncit:C7057 .
  
  dgn-gda:DGNca39b12aaf2138ca64204806066c9c82 sio:SIO_000628 miriam-gene:7157, lld:C0006413;
    a sio:SIO_001121 .
}

dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_provenance {
  dgn-np:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_assertion dcterms:description
      "[Recent studies of the p53 gene in Burkitt's lymphomas have demonstrated that mutations are extremely common, and in fact it is rare that both alleles of the p53 gene in these tumors are not inactivated by mutation or deletion.]. 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:1437144;
    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:NP288289.RAG4aOBzwLG5J8TrxR4Ft4rMIRsPT2wRSoSJLJauJuV1o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:44+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" .
}