@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw> .
@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:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_head {
  this: np:hasAssertion dgn-np:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_assertion;
    np:hasProvenance dgn-np:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_provenance;
    np:hasPublicationInfo dgn-np:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_assertion a np:Assertion .
  
  dgn-np:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_provenance a np:Provenance .
  
  dgn-np:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0206754 a ncit:C7057 .
  
  dgn-gda:DGN77c61f3840ea76a53dc82fb5cd5e918d sio:SIO_000628 miriam-gene:1956, lld:C0206754;
    a sio:SIO_001121 .
}

dgn-np:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_provenance {
  dgn-np:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_assertion dcterms:description
      "[For example, foregut NETs have frequent deletions and mutations of the MEN1 gene, whereas midgut NETs have losses of chromosome 18, 11q and 16q and hindgut NETs express transforming growth factor-alpha and the epidermal growth factor receptor.]. 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:14713256;
    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:NP369384.RAddE1ZYyFA4Zv3Dzd0pNH6mC85JnT8dVsBgK6TrZu6sw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:13+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" .
}