@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8> .
@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:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_head {
  this: np:hasAssertion dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_assertion;
    np:hasProvenance dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_provenance;
    np:hasPublicationInfo dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_assertion a np:Assertion .
  
  dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_provenance a np:Provenance .
  
  dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_assertion {
  miriam-gene:2475 a ncit:C16612 .
  
  lld:C0238462 a ncit:C7057 .
  
  dgn-gda:DGNefd548272928e4fcf445c121dc5e93d8 sio:SIO_000628 miriam-gene:2475, lld:C0238462;
    a sio:SIO_001121 .
}

dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_provenance {
  dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_assertion dcterms:description
      "[In addition, the recent findings of H-RAS mutations in 56% of RET-negative sporadic MTC and the activation of the mammalian target of rapamycin (mTOR) intracellular signaling pathway in hereditary MTC suggests that additional or alternative genetic events are important for MTC pathogenesis.]. 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:22343387;
    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:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:37+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" .
}