@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI> .
@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:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_head {
  this: np:hasAssertion dgn-np:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_assertion;
    np:hasProvenance dgn-np:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_provenance;
    np:hasPublicationInfo dgn-np:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_assertion a np:Assertion .
  
  dgn-np:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_provenance a np:Provenance .
  
  dgn-np:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0007194 a ncit:C7057 .
  
  dgn-gda:DGN9a781748a923acbbb6a2344bd8e7ba19 sio:SIO_000628 miriam-gene:183, lld:C0007194;
    a sio:SIO_001121 .
}

dgn-np:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_provenance {
  dgn-np:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_assertion dcterms:description
      "[The angiotensin II type 1 receptor (AT-1) mediates the major pressor and trophic actions of angiotensin II (Ang II) and at least 50 different polymorphisms have been described in the AT-1 gene (AT(1)R gene); in particular, the C allele of the +1166A/C polymorphism has been associated with the severe form of essential hypertension, but the role of this polymorphism is still ambiguous in pathologies related to high Ang II levels, such as deterioration of renal function, arterial stiffness and hypertrophic cardiomyopathy.]. 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:15640279;
    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:NP887065.RAka5mghjVfRqWmAHVFjTvagJ9Tb2PV34YZLHypW1jUQI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:04+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" .
}