@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg> .
@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:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_head {
  this: np:hasAssertion dgn-np:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_assertion;
    np:hasProvenance dgn-np:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_provenance;
    np:hasPublicationInfo dgn-np:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_assertion a np:Assertion .
  
  dgn-np:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_provenance a np:Provenance .
  
  dgn-np:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_assertion {
  miriam-gene:1257 a ncit:C16612 .
  
  lld:C0406810 a ncit:C7057 .
  
  dgn-gda:DGNaa6d3d6c17690cc4a857a084a1795de4 sio:SIO_000628 miriam-gene:1257, lld:C0406810;
    a sio:SIO_001121 .
}

dgn-np:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_provenance {
  dgn-np:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_assertion dcterms:description
      "[As somatotropinomas are the predominant pituitary tumor subtype associated with CNC and arise before 30 yr of age, which is strikingly similar to the age at diagnosis for IFS, we explored the possibility that the putative CNC genes might also contribute to the pathogenesis of IFS.]. 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:10690880;
    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:NP858020.RArRCZ-U-kEag1jQE6kGcduSr53VEye5A8wuMCFaGdLXg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:44+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" .
}