@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8> .
@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:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_head {
  this: np:hasAssertion dgn-np:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_assertion;
    np:hasProvenance dgn-np:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_provenance;
    np:hasPublicationInfo dgn-np:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_assertion a np:Assertion .
  
  dgn-np:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_provenance a np:Provenance .
  
  dgn-np:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0022658 a ncit:C7057 .
  
  dgn-gda:DGNec1aaee2e88fd0fa2586e03e02922bd5 sio:SIO_000628 miriam-gene:183, lld:C0022658;
    a sio:SIO_001121 .
}

dgn-np:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_provenance {
  dgn-np:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_assertion dcterms:description
      "[Two alleles of the microsatellite marker adjacent to the angiotensinogen gene were less common among nephropathy cases than among controls, but this was not significant when controlling for the same variables as above.]. 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:18413189;
    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:NP189887.RAAGHHQISonkIE413NPofTmWu9q5vqmAU7uzzps9SmKG8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+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" .
}