@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU> .
@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/v4.0.0/void/> .

dgn-np:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_head {
  this: np:hasAssertion dgn-np:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_assertion;
    np:hasProvenance dgn-np:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_provenance;
    np:hasPublicationInfo dgn-np:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_assertion a np:Assertion .
  
  dgn-np:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_provenance a np:Provenance .
  
  dgn-np:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  
  lld:C0031511 a ncit:C7057 .
  
  dgn-gda:DGNc9494fb031caf9e8661276fe132ff7b4 sio:SIO_000628 miriam-gene:7428, lld:C0031511;
    a sio:SIO_001121 .
}

dgn-np:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_provenance {
  dgn-np:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_assertion dcterms:description
      "[However, on genotyping a group of 172 sporadic or familial pheochromocytomas, we characterized four unrelated probands with familial pheochromocytomas without any sequence variants of RET (exons 8, 10, 11, 13, 14, 15, and 16) or the entire coding sequence of VHL, SDHB, SDHC, SDHD, and EGLN3 (exon-intron boundaries included).]. 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:17102081;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP579157.RA5SbWqPoN7BF1TrAPC2y689ckmPgCOa2RKCK901u6nWU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:07+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}