@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q> .
@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:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_head {
  this: np:hasAssertion dgn-np:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_assertion;
    np:hasProvenance dgn-np:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_provenance;
    np:hasPublicationInfo dgn-np:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_assertion a np:Assertion .
  
  dgn-np:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_provenance a np:Provenance .
  
  dgn-np:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_assertion {
  miriam-gene:7015 a ncit:C16612 .
  
  lld:C0027819 a ncit:C7057 .
  
  dgn-gda:DGNa9506cbe2323719b93341a419edce22c sio:SIO_000628 miriam-gene:7015, lld:C0027819;
    a sio:SIO_001121 .
}

dgn-np:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_provenance {
  dgn-np:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_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:NP728425.RAAPF2lsP3O9rImsgmF32enbtCHvqj8ImvlCUKbq8PQ5Q130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:59+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" .
}