@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao> .
@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:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_head {
  this: np:hasAssertion dgn-np:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_assertion;
    np:hasProvenance dgn-np:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_provenance;
    np:hasPublicationInfo dgn-np:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_assertion a np:Assertion .
  
  dgn-np:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_provenance a np:Provenance .
  
  dgn-np:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_assertion {
  miriam-gene:6750 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGN8222f02d11de84a8928096e059eeb5f2 sio:SIO_000628 miriam-gene:6750, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_provenance {
  dgn-np:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_assertion dcterms:description
      "[The presence of these SST receptor subtypes in human ovarian cancers allows the use of SST analogs and their radionuclide and cytotoxic derivatives for the diagnosis and treatment of this malignancy.]. 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:11061491;
    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:NP235199.RAeo0NS_jMUzg-nIGSyc5EP8ezX0J7DnNB2_XVaz-xdao130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:12+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" .
}