@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc> .
@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:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_head {
  this: np:hasAssertion dgn-np:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_assertion;
    np:hasProvenance dgn-np:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_provenance;
    np:hasPublicationInfo dgn-np:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_assertion a np:Assertion .
  
  dgn-np:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_provenance a np:Provenance .
  
  dgn-np:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  
  lld:C0877373 a ncit:C7057 .
  
  dgn-gda:DGNc0d6fb831a4d48def7cc611cb4b514bf sio:SIO_000628 miriam-gene:3845, lld:C0877373;
    a sio:SIO_001121 .
}

dgn-np:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_provenance {
  dgn-np:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_assertion dcterms:description
      "[The CIMP-H MLH1 methylation-negative subtype exhibited elevated incidence rates in male patients and was associated with larger tumor size, more frequent loss of MSH2 expression, increased frequency of KRAS mutation, and advanced cancer stage.]. 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:23370766;
    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:NP612806.RASdggTE0h4z73eAQuYxmmI0aGpVJ1M_1eAt7QNr2f-lc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:10+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" .
}