@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg> .
@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/v4.0.0/void/> .
dgn-np:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_head {
  this: np:hasAssertion dgn-np:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_assertion ;
    np:hasProvenance dgn-np:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_provenance ;
    np:hasPublicationInfo dgn-np:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_assertion a np:Assertion .
  dgn-np:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_provenance a np:Provenance .
  dgn-np:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0023418 a ncit:C7057 .
  dgn-gda:DGN47b690d3a670f9e0248d5a163af2d535 sio:SIO_000628 miriam-gene:7157 , lld:C0023418 ;
    a sio:SIO_001121 .
}
dgn-np:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_provenance {
  dgn-np:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_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 &gt; 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-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1379629.RASj1YhepSRhm8nExlVLQE-zKdCKbx9YUHOcrYTVS2TRg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:11+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}