@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0> .
@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:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_head {
  this: np:hasAssertion dgn-np:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_assertion;
    np:hasProvenance dgn-np:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_provenance;
    np:hasPublicationInfo dgn-np:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_assertion a np:Assertion .
  
  dgn-np:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_provenance a np:Provenance .
  
  dgn-np:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0206754 a ncit:C7057 .
  
  dgn-gda:DGNf0d61f6d249ec676da6e9067b3fc49cb sio:SIO_000628 miriam-gene:7157, lld:C0206754;
    a sio:SIO_001121 .
}

dgn-np:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_provenance {
  dgn-np:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_assertion dcterms:description
      "[As the neoplasia investigated in this study comprised a wide spectrum of neuroendocrine tumour types and ranged from minute, relatively benign lesions to malignant metastasizing disease and as there was no relationship between the presence of p53 overexpression and clinico-pathological features, the present study suggests that p53 gene mutation may be relatively unimportant in the genesis of neuroendocrine tumours.]. 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:7790993;
    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:NP401736.RADze31ZIqRaIGYxF01AzryocrZNSHVlzkxIKnMFBOeh0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:59+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: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" .
}