@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs> .
@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:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_head {
   this: np:hasAssertion dgn-np:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_assertion ;
    np:hasProvenance dgn-np:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_provenance ;
    np:hasPublicationInfo dgn-np:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_assertion a np:Assertion .
  dgn-np:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_provenance a np:Provenance .
  dgn-np:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_assertion {
   miriam-gene:1462 a ncit:C16612 .
  lld:C0007134 a ncit:C7057 .
  dgn-gda:DGN0b30fd0bf2ad98765c0305bb0cda1cc7 sio:SIO_000628 miriam-gene:1462 , lld:C0007134 ;
    a sio:SIO_001121 .
}
dgn-np:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_provenance {
   dgn-np:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_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:NP227116.RA5abNkh7-XHZ6E8L1Yq_Kxnfl7e64TuqySP4E4bI90fs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:06+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" .
}