@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw> .
@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:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_head {
  this: np:hasAssertion dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_assertion;
    np:hasProvenance dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_provenance;
    np:hasPublicationInfo dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_assertion a np:Assertion .
  
  dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_provenance a np:Provenance .
  
  dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_assertion {
  miriam-gene:673 a ncit:C16612 .
  
  lld:C0206754 a ncit:C7057 .
  
  dgn-gda:DGN262050fd773f065433e2d1aea7778fa5 sio:SIO_000628 miriam-gene:673, lld:C0206754;
    a sio:SIO_001121 .
}

dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_provenance {
  dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_assertion dcterms:description
      "[We compared clinicopathological features and loss of heterozygosity of chromosomes 11q, 16q and 18, and BRAF gene mutations in 47 patients with neuroendocrine tumors including 16 with pancreatic endocrine tumors, 15 with nonileal carcinoid tumors and 16 with ileal carcinoid tumors.]. 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:15920555;
    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:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:48+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" .
}