@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo> .
@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:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_head {
  this: np:hasAssertion dgn-np:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_assertion;
    np:hasProvenance dgn-np:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_provenance;
    np:hasPublicationInfo dgn-np:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_assertion a np:Assertion .
  
  dgn-np:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_provenance a np:Provenance .
  
  dgn-np:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_assertion {
  miriam-gene:4893 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNf19f6bccbb0e478ed79448897c7ff402 sio:SIO_000628 miriam-gene:4893, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_provenance {
  dgn-np:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_assertion dcterms:description
      "[Using a collection of 225 colorectal cancers from 2 prospective cohort studies, we examined the relationship between NRAS mutations, clinical outcome, and other molecular features, including mutation of KRAS, BRAF, and PIK3CA, microsatellite instability, and the CpG island methylator phenotype.]. 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:20736745;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP83734.RALSNyytu7Syw5OVlYpSHva4T9y5lSSKo7-DIn1CC4xdo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:41+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" .
}