@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w> .
@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:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_head {
  this: np:hasAssertion dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_assertion;
    np:hasProvenance dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_provenance;
    np:hasPublicationInfo dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_assertion a np:Assertion .
  
  dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_provenance a np:Provenance .
  
  dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_assertion {
  miriam-gene:3643 a ncit:C16612 .
  
  lld:C0085580 a ncit:C7057 .
  
  dgn-gda:DGNbf38e51368725be0edfec43fb4b0e5d9 sio:SIO_000628 miriam-gene:3643, lld:C0085580;
    a sio:SIO_001121 .
}

dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_provenance {
  dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_assertion dcterms:description
      "[To determine whether a microsatellite polymorphism of the insulin receptor gene (INSR) is associated with essential hypertension, as has been demonstrated previously for an RsaI restriction fragment length polymorphism (RFLP), and to examine blood pressure and plasma lipid profiles in relation to genotype.]. 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:7769500;
    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:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:15+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" .
}