@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI> .
@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:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_head {
  this: np:hasAssertion dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_assertion;
    np:hasProvenance dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_provenance;
    np:hasPublicationInfo dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_assertion a np:Assertion .
  
  dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_provenance a np:Provenance .
  
  dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_assertion {
  miriam-gene:6390 a ncit:C16612 .
  
  lld:C0031511 a ncit:C7057 .
  
  dgn-gda:DGN0dccf88c485e11ae3b3ee2b03fcaa788 sio:SIO_000628 miriam-gene:6390, lld:C0031511;
    a sio:SIO_001121 .
}

dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_provenance {
  dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_assertion dcterms:description
      "[In the last few years several papers have reported on the association between mutations of the genes encoding the structural (SDHC, SDHD) and catalytic (SDHB) subunits of succinate dehydrogenase and the occurrence of hereditary pheochromocytomas/paragangliomas (Pheo/PGL) syndromes.]. 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:19411806;
    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:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:32+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" .
}