@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo> .
@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:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_head {
  this: np:hasAssertion dgn-np:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_assertion;
    np:hasProvenance dgn-np:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_provenance;
    np:hasPublicationInfo dgn-np:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_assertion a np:Assertion .
  
  dgn-np:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_provenance a np:Provenance .
  
  dgn-np:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_assertion {
  miriam-gene:100 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNb69fb1e16cab690948c76cf646018b19 sio:SIO_000628 miriam-gene:100, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_provenance {
  dgn-np:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_assertion dcterms:description
      "[ The adenosine-related gene variants do not appear to alter susceptibility to the disease in this group of essential hypertensives. However, involvement of these genes and the adenosine system cannot be conclusively excluded from essential hypertension pathogenesis as other gene variants may still be involved.]. 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:15257174;
    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:NP49319.RA-8QiNX2TVQLlUMSrzAh0jyrI2WWVUl5V6ztOwAHsbYo130_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" .
}