@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI> .
@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:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_head {
  this: np:hasAssertion dgn-np:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_assertion;
    np:hasProvenance dgn-np:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_provenance;
    np:hasPublicationInfo dgn-np:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_assertion a np:Assertion .
  
  dgn-np:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_provenance a np:Provenance .
  
  dgn-np:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_assertion {
  miriam-gene:673 a ncit:C16612 .
  
  lld:C0699790 a ncit:C7057 .
  
  dgn-gda:DGN976ea1870b183d571c4d074c003eb44d sio:SIO_000628 miriam-gene:673, lld:C0699790;
    a sio:SIO_001121 .
}

dgn-np:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_provenance {
  dgn-np:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_assertion dcterms:description
      "[In this issue of Cancer Cell, Rad and colleagues report findings that underscore the importance of oncogenic BRAF mutation coupled with microsatellite instability, p16Ink4a inactivation, and p53 mutation in the serrated pathway of colon cancer development.]. 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:23845435;
    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:NP219982.RAa5eRv5w8BsXNCvkakctmeRxKqWVfTAzdXkMhPh1WlnI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:02+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" .
}