@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o> .
@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:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_head {
  this: np:hasAssertion dgn-np:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_assertion;
    np:hasProvenance dgn-np:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_provenance;
    np:hasPublicationInfo dgn-np:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_assertion a np:Assertion .
  
  dgn-np:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_provenance a np:Provenance .
  
  dgn-np:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_assertion {
  miriam-gene:55856 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGN3fb3bdea52ed0f9b2bb49181f667d322 sio:SIO_000628 miriam-gene:55856, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_provenance {
  dgn-np:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_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:NP776154.RAXNWTcNJFVFGwhCb4TzBp04tCt5_Y6Wpx4aYnhe7Qp5o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:50+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" .
}