@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI> .
@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:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_head {
  this: np:hasAssertion dgn-np:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_assertion;
    np:hasProvenance dgn-np:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_provenance;
    np:hasPublicationInfo dgn-np:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_assertion a np:Assertion .
  
  dgn-np:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_provenance a np:Provenance .
  
  dgn-np:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0279626 a ncit:C7057 .
  
  dgn-gda:DGNdf26582490df725fdfb420b1f7c2c695 sio:SIO_000628 miriam-gene:7157, lld:C0279626;
    a sio:SIO_001121 .
}

dgn-np:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_provenance {
  dgn-np:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_assertion dcterms:description
      "[Comparison with published results from other geographic areas of high SCCE incidence revealed that the spectrum of TP53 mutations in south Thailand is similar to that observed in central China (Henan Province) but clearly differs from that of SCCE from western Europe (Normandy, France; northern Italy), with more G:T transversions and fewer mutations affecting A and T base pairs.]. 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:11004672;
    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:NP193746.RA7EmNjsMAiMIgUCiTMY1dFTHN_El8ENxFJ4izih7GBUI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:46+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" .
}