@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0> .
@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:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_head {
  this: np:hasAssertion dgn-np:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_assertion;
    np:hasProvenance dgn-np:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_provenance;
    np:hasPublicationInfo dgn-np:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_assertion a np:Assertion .
  
  dgn-np:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_provenance a np:Provenance .
  
  dgn-np:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_assertion {
  miriam-gene:10993 a ncit:C16612 .
  
  lld:C0030421 a ncit:C7057 .
  
  dgn-gda:DGN50ae2fde4c74c9adfca5a33eef182726 sio:SIO_000628 miriam-gene:10993, lld:C0030421;
    a sio:SIO_001121 .
}

dgn-np:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_provenance {
  dgn-np:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_assertion dcterms:description
      "[Germline mutations in three of the succinate dehydrogenase (SDH, mitochondrial complex II) subunits (SDHD, SDHB and SDHC) cause susceptibility to head and neck paragangliomas, and may be found in approximately 20% of unselected patients.]. 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:12351569;
    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:NP173635.RAt_mhSaklPTUG-0zhVhYgfyL_q5XVcJWDTWaatdfOhe0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:34+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" .
}