@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts> .
@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:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_head {
   this: np:hasAssertion dgn-np:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_assertion ;
    np:hasProvenance dgn-np:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_provenance ;
    np:hasPublicationInfo dgn-np:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_assertion a np:Assertion .
  dgn-np:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_provenance a np:Provenance .
  dgn-np:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_assertion {
   miriam-gene:5243 a ncit:C16612 .
  lld:C0007134 a ncit:C7057 .
  dgn-gda:DGN7ed17fc19580a34dc3ad80244c7cdb99 sio:SIO_000628 miriam-gene:5243 , lld:C0007134 ;
    a sio:SIO_001121 .
}
dgn-np:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_provenance {
   dgn-np:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_assertion dcterms:description "[These genes (ACY1, WT1, SELENBP1, COBL, EFHD1, AGXT2L1, ALDH5A1, THEM2, ABCB1, FLJ14146, CSPG2, TRIM9 and HEY1) are good candidates for genes whose activity is changed upon the decrease of HNF4alpha in RCC.]. 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:16007190 ;
    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:NP694498.RAHWV7OCOYOHd66dnO9tilYLs74HCgaxUu2ib0RViIsts130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:02+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" .
}