@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc> .
@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 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:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_head {
  this: np:hasAssertion dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_assertion;
    np:hasProvenance dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_provenance;
    np:hasPublicationInfo dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_assertion a np:Assertion .
  
  dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_provenance a np:Provenance .
  
  dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0038356 a ncit:C7057 .
  
  dgn-gda:DGNdcfe3f222e9fed5aabf34b13032d3e9a sio:SIO_000628 miriam-gene:7157, lld:C0038356;
    a sio:SIO_001122 .
}

dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_provenance {
  dgn-np:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_assertion dc:description
      "[this study suggests that the p53 codon 72 polymorphism may be associated with gastric cancer in Chinese Han patients, and that difference in genotype distribution may be associated with the location and stage of gastric cancer.]. 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:20939739;
    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:NP80282.RAZJaEndlAnBu334yXrU0O4jj2A051r0uGkCkG6wLguuc130_publicationInfo {
  this: dc:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}