@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8> .
@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:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_head {
  this: np:hasAssertion dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion;
    np:hasProvenance dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance;
    np:hasPublicationInfo dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion a np:Assertion .
  
  dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance a np:Provenance .
  
  dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion {
  miriam-gene:113675 a ncit:C16612 .
  
  lld:C0030421 a ncit:C7057 .
  
  dgn-gda:DGN01e4c24717b9701467bce6ad376d7fa1 sio:SIO_000628 miriam-gene:113675, lld:C0030421;
    a sio:SIO_001121 .
}

dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance {
  dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion dcterms:description
      "[Approximately 10% to 15% of paragangliomas are caused by mutations in the succinate dehydrogenase (SDH) genes B, C, or D. These are often multifocal as part of paraganglioma syndromes and hormone secreting, and malignant particularly associated with mutations in SDHB.]. 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:18213727;
    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:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:51+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" .
}