@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo> .
@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:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_head {
  this: np:hasAssertion dgn-np:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_assertion;
    np:hasProvenance dgn-np:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_provenance;
    np:hasPublicationInfo dgn-np:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_assertion a np:Assertion .
  
  dgn-np:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_provenance a np:Provenance .
  
  dgn-np:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0232197 a ncit:C7057 .
  
  dgn-gda:DGN6628fafeeb0faa9cdef2aa52379ca7f9 sio:SIO_000628 miriam-gene:183, lld:C0232197;
    a sio:SIO_001121 .
}

dgn-np:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_provenance {
  dgn-np:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_assertion dcterms:description
      "[This study demonstrates the association of RAS gene polymorphisms with nonfamilial structural AF and may provide the rationale for clinical trials to investigate the use of ACE inhibitor or angiotensin II antagonist in the treatment of structural AF.]. 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:15023884;
    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:NP855543.RAzfl1lJ5dtBs4V_kaSrXZtgSZckEJeWMFMMqQ1f33UVo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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" .
}