@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc> .
@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:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_head {
  this: np:hasAssertion dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_assertion;
    np:hasProvenance dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_provenance;
    np:hasPublicationInfo dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_assertion a np:Assertion .
  
  dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_provenance a np:Provenance .
  
  dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN8e379806b432de2b09564e4aa82aaf70 sio:SIO_000628 miriam-gene:7157, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_provenance {
  dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_assertion dcterms:description
      "[We genotyped p53 codon 72 in 193 individuals with Lynch syndrome mutations, 93 patients with sporadic microsatellite unstable colorectal cancer, and 93 patients with sporadic microsatellite stable colorectal cancer from Finland and 323 Finnish controls.]. 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:16203772;
    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:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:24+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" .
}