@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ> .
@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:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_head {
  this: np:hasAssertion dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_assertion ;
    np:hasProvenance dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_assertion a np:Assertion .
  dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_provenance a np:Provenance .
  dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  lld:C0149721 a ncit:C7057 .
  dgn-gda:DGN999703cd6c69df2042bfaaea29cb1c82 sio:SIO_000628 miriam-gene:3630 , lld:C0149721 ;
    a sio:SIO_001121 .
}
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_provenance {
  dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_assertion dcterms:description "[The mechanisms through which hypertension contributes to the occurrence of myocardial infarction should be discussed from two points of view: (1) common risk factors for the two diseases, such as genetic risk, insulin resistance, sympathetic hyperactivity, and vasoactive substances such as angiotensin K, and (2) linking factors that are induced by hypertension and contribute to the development of atherosclerosis and myocardial infarction, such as atherosclerosis and left ventricular hypertrophy.]. 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:8677859 ;
    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:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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" .
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}