@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_head {
  this: np:hasAssertion dgn-np:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_assertion;
    np:hasProvenance dgn-np:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_provenance;
    np:hasPublicationInfo dgn-np:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_assertion a np:Assertion .
  
  dgn-np:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_provenance a np:Provenance .
  
  dgn-np:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_assertion {
  miriam-gene:5290 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNb4c57ef85525038c29e10521f68de202 sio:SIO_000628 miriam-gene:5290, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_provenance {
  dgn-np:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_assertion dcterms:description
      "[This is the first report on CRC in Malaysia showing comparable frequency of KRAS mutation and PTEN loss, lower BRAF mutation rate, higher PIK3CA amplification frequency, and rare PTEN mutation, as compared with published reports.]. 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:23992303;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1106682.RAVn6EQSX9rz_ZVy8EFoSRYJga7lipOskwTJWOrGJo4ss130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:07+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}