@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8> .
@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:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_head {
  this: np:hasAssertion dgn-np:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_assertion;
    np:hasProvenance dgn-np:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_provenance;
    np:hasPublicationInfo dgn-np:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_assertion a np:Assertion .
  
  dgn-np:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_provenance a np:Provenance .
  
  dgn-np:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_assertion {
  miriam-gene:112399 a ncit:C16612 .
  
  lld:C0031511 a ncit:C7057 .
  
  dgn-gda:DGNc7f706c8b40bffd427604d1d1ffb72de sio:SIO_000628 miriam-gene:112399, lld:C0031511;
    a sio:SIO_001121 .
}

dgn-np:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_provenance {
  dgn-np:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_assertion dcterms:description
      "[Although other molecular mechanisms, such as particular variants in untranslated regions or partial gene deletions, cannot be ruled out, we think finding families with nonsyndromic pheochromocytoma without any RET, VHL, SDHB, SDHC, SDHD, or EGLN3 mutation may argue in favor of the presence of other pheochromocytoma susceptibility genes.]. 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:NP579156.RAAvghb4Hkx9dTFCDefB-l59_IeEyrwBlN1Q8erDKk0a8130_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" .
}