@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c> .
@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:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_head {
   this: np:hasAssertion dgn-np:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_assertion ;
    np:hasProvenance dgn-np:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_provenance ;
    np:hasPublicationInfo dgn-np:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_assertion a np:Assertion .
  dgn-np:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_provenance a np:Provenance .
  dgn-np:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_assertion {
   miriam-gene:6392 a ncit:C16612 .
  lld:C0030421 a ncit:C7057 .
  dgn-gda:DGNf618b6e3e240117adfcf3a284871a646 sio:SIO_000628 miriam-gene:6392 , lld:C0030421 ;
    a sio:SIO_001121 .
}
dgn-np:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_provenance {
   dgn-np:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_assertion dcterms:description "[Three patients with PHEO (2F-, 1F+) presented VHL mutations (P86A, G93C, and R167W), six with PGL (4F-, 2F+) were positive for SDH or VHL mutations (SDHB R230G in two patients, SDHB S8F, R46Q, R90Q, and VHL P81L in one subject each), and one with hnPGL carried the SDHD 348-351delGACT mutation.]. 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:17102082 ;
    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:NP163402.RA3EZMopWHGzu07TAZfvkxwwZSeN_-wdFguvIVXG6SX7c130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:28+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" .
}