@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA> .
@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:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_head {
  this: np:hasAssertion dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_assertion ;
    np:hasProvenance dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_provenance ;
    np:hasPublicationInfo dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_assertion a np:Assertion .
  dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_provenance a np:Provenance .
  dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  lld:C0022658 a ncit:C7057 .
  dgn-gda:DGN0dbb49063c80ade7ca1ea5aa6dcf8439 sio:SIO_000628 miriam-gene:1636 , lld:C0022658 ;
    a sio:SIO_001122 .
}
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_provenance {
  dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_assertion dcterms:description "[In our studies on the hypertension in kidney disease we have choosen the evaluation of incidence of hypertension in the early stage of primary glomerulonephritis (GN) and the comparison of distribution of genotypes and alleles depending on insertion/deletion polymorphism of angiotensin converting enzyme (ACE) gene in patients with early stage of GN and healthy subjects.]. 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:14974362 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}