@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ> .
@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:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_head {
  this: np:hasAssertion dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_assertion;
    np:hasProvenance dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_provenance;
    np:hasPublicationInfo dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_assertion a np:Assertion .
  
  dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_provenance a np:Provenance .
  
  dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN65cd0e6a00376b7d42322a182da5c994 sio:SIO_000628 miriam-gene:5728, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_provenance {
  dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_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:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_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" .
}