@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo> .
@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:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_head {
  this: np:hasAssertion dgn-np:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_assertion;
    np:hasProvenance dgn-np:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_provenance;
    np:hasPublicationInfo dgn-np:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_assertion a np:Assertion .
  
  dgn-np:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_provenance a np:Provenance .
  
  dgn-np:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0023452 a ncit:C7057 .
  
  dgn-gda:DGN2734b121794f53affe39e7a5b85d0c45 sio:SIO_000628 miriam-gene:7157, lld:C0023452;
    a sio:SIO_001121 .
}

dgn-np:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_provenance {
  dgn-np:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_assertion dcterms:description
      "[To investigate its relevance in childhood acute lymphoblastic leukemia (ALL) susceptibility, we genotyped 114 cases and 414 newborn controls from Wales (UK) for polymorphisms in TP53 (R72P), its negative regulator MDM2 (single-nucleotide polymorphism SNP309, rs2279744), and selected HLA complex genes whose products interact with TP53.]. 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:19837266;
    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:NP200127.RAN8fjK5rOyXDvYX1VyQx7exIcAqYFYR5MVsNVdCmW1eo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:50+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" .
}