@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI> .
@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/v3.0.0/void/> .

dgn-np:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_head {
  this: np:hasAssertion dgn-np:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_assertion;
    np:hasProvenance dgn-np:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_provenance;
    np:hasPublicationInfo dgn-np:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_assertion a np:Assertion .
  
  dgn-np:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_provenance a np:Provenance .
  
  dgn-np:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_assertion {
  miriam-gene:7253 a ncit:C16612 .
  
  lld:C0027819 a ncit:C7057 .
  
  dgn-gda:DGNfb3d577c29a0d53a331eb943c2c4e114 sio:SIO_000628 miriam-gene:7253, lld:C0027819;
    a sio:SIO_001121 .
}

dgn-np:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_provenance {
  dgn-np:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_assertion dcterms:description
      "[The most common point mutations involved the neuroblastoma RAS viral oncogene homolog (NRAS), followed by the Kirsten rat sarcoma viral oncogene homolog (KRAS), the telomerase reverse transcriptase (TERT) gene, and the thyroid-stimulating hormone receptor (TSHR) gene.]. 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:25209362;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP760567.RA2y1W52az2W_YphLWd3bKLdfyPjeQ9OpSJ5RXZFGGVmI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:19+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}