@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24> .
@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:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_head {
  this: np:hasAssertion dgn-np:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_assertion;
    np:hasProvenance dgn-np:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_provenance;
    np:hasPublicationInfo dgn-np:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_assertion a np:Assertion .
  
  dgn-np:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_provenance a np:Provenance .
  
  dgn-np:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0149721 a ncit:C7057 .
  
  dgn-gda:DGNc9a01ebe7aef6c330eb1a423b4bc0917 sio:SIO_000628 miriam-gene:4846, lld:C0149721;
    a sio:SIO_001122 .
}

dgn-np:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_provenance {
  dgn-np:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_assertion dcterms:description
      "[These findings, not previously described, provide important preliminary evidence to suggest an increased susceptibility to LVH in African Americans who carry the 894T variant of the eNOS gene and have high-normal blood pressure.]. 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:15712782;
    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:NP61800.RANviQCtNhlsSGSKxlv5gp9RtggwtLrmnJ6xkX6pLlp24130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}