@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas> .
@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:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_head {
  this: np:hasAssertion dgn-np:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_assertion ;
    np:hasProvenance dgn-np:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_provenance ;
    np:hasPublicationInfo dgn-np:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_assertion a np:Assertion .
  dgn-np:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_provenance a np:Provenance .
  dgn-np:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_assertion {
  miriam-gene:185 a ncit:C16612 .
  lld:C0020456 a ncit:C7057 .
  dgn-gda:DGN8838244beb51d5d8939d5f5dac4ecf36 sio:SIO_000628 miriam-gene:185 , lld:C0020456 ;
    a sio:SIO_001121 .
}
dgn-np:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_provenance {
  dgn-np:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_assertion dcterms:description "[Because hypertension and renal hemodynamic function are also related to the risk of diabetic nephropathy and because hyperglycemia can activate the renin angiotensin system, we sought to determine if there is an association between the AGT1R polymorphism, baseline renal and peripheral hemodynamic function, and pressor response to high glucose in subjects with early uncomplicated type 1 diabetes.]. 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:10969844 ;
    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:NP777308.RAHmRBYo2IGTCIgwPH2zP9R0c9LWqAUYoj_YJjeZSqZas130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:51+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> ;
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}