@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM> .
@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:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_head {
  this: np:hasAssertion dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_assertion;
    np:hasProvenance dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_provenance;
    np:hasPublicationInfo dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_assertion a np:Assertion .
  
  dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_provenance a np:Provenance .
  
  dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0546837 a ncit:C7057 .
  
  dgn-gda:DGNa7697788cd4096df18dd169c81a35679 sio:SIO_000628 miriam-gene:7157, lld:C0546837;
    a sio:SIO_001122 .
}

dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_provenance {
  dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_assertion dcterms:description
      "[This study aimed to evaluate the prognostic significance of two functional single nucleotide polymorphisms (SNP) in the p53 pathway (p53 Arg72Pro and MDM2 T309G) in patients with esophageal cancer, and to determine the importance of histologic subtype in the SNP-outcome relationships.]. 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:19383811;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}