@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE> .
@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:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_head {
  this: np:hasAssertion dgn-np:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_assertion ;
    np:hasProvenance dgn-np:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_provenance ;
    np:hasPublicationInfo dgn-np:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_assertion a np:Assertion .
  dgn-np:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_provenance a np:Provenance .
  dgn-np:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_assertion {
  miriam-gene:4193 a ncit:C16612 .
  lld:C0220621 a ncit:C7057 .
  dgn-gda:DGN15fcf7588739b86ee26c9f6953c95fcc sio:SIO_000628 miriam-gene:4193 , lld:C0220621 ;
    a sio:SIO_001121 .
}
dgn-np:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_provenance {
  dgn-np:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_assertion dcterms:description "[To investigate a potential role for MDM2 in the inactivation of wt-p53 in pediatric acute lymphoblastic leukemia (ALL), we examined the expression of MDM2 and p53, as well as the occurrence of p53 mutations and possible amplification of the MDM2 gene, in 19 pediatric ALL cell lines and one pediatric acute myelogenous leukemia (AML) line.]. 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:7888679 ;
    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:NP819732.RAicMz1rHlvf2gdYcSBKtg-PsjTi4NHRv1RKC-9ANbbHE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:22+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" .
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}