@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg> .
@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:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_head {
  this: np:hasAssertion dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_assertion;
    np:hasProvenance dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_provenance;
    np:hasPublicationInfo dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_assertion a np:Assertion .
  
  dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_provenance a np:Provenance .
  
  dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNc609be30adc9928bdb9f5df70cfa77cf sio:SIO_000628 miriam-gene:3845, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_provenance {
  dgn-np:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_assertion dcterms:description
      "[Specific KRAS mutation is an informative prognostic factor in both sporadic and hereditary CRC and applied in an algorithm with BRAF(V600E) and MSI may identify sporadic CRC patients with poor clinical outcome.]. 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:20162668;
    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:NP794332.RAsMrS5u7ifN3goLJrdK4FjtOjNY2EI1YZfQTSS7icmEg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:45+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" .
}