@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY> .
@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:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_head {
  this: np:hasAssertion dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_assertion ;
    np:hasProvenance dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_provenance ;
    np:hasPublicationInfo dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_assertion a np:Assertion .
  dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_provenance a np:Provenance .
  dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0023449 a ncit:C7057 .
  dgn-gda:DGNc4b8d4b2d360fd1a26da6c2441cf7427 sio:SIO_000628 miriam-gene:7157 , lld:C0023449 ;
    a sio:SIO_001121 .
}
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_provenance {
  dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_assertion dcterms:description "[p53 mutations predominated in lymphoid leukaemia and were several fold more frequent in leukaemia in relapse than in the de novo disease, were associated with loss of the normal p53 allele (monosomy 17) in > 50% of cases and carried a poor prognosis in AML, MDS and chronic lymphatic leukaemia and a 3.8-fold increase risk of death in T cell acute lymphocytic leukaemia.]. 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:9279367 ;
    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:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:26+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" .
}