@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8> .
@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:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_head {
  this: np:hasAssertion dgn-np:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_assertion;
    np:hasProvenance dgn-np:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_provenance;
    np:hasPublicationInfo dgn-np:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_assertion a np:Assertion .
  
  dgn-np:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_provenance a np:Provenance .
  
  dgn-np:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_assertion {
  miriam-gene:2056 a ncit:C16612 .
  
  lld:C1142276 a ncit:C7057 .
  
  dgn-gda:DGN350fd69df25c1b0b818cf716f951d8b0 sio:SIO_000628 miriam-gene:2056, lld:C1142276;
    a sio:SIO_001121 .
}

dgn-np:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_provenance {
  dgn-np:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_assertion dcterms:description
      "[The association of the angiotensinogen (AGT) gene variation at codon 235, the T235 variant, with hypertension induced by erythropoietin (Epo) was investigated in patients with progressive renal disease requiring treatment for renal anemia with Epo.]. 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:11675943;
    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:NP597009.RAp7yN2s9Iw_Yx7Ci4zfVIeqJDY1_kq6c5ZctDS8xaMg8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:59+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" .
}