@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU> .
@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:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_head {
  this: np:hasAssertion dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_assertion ;
    np:hasProvenance dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_provenance ;
    np:hasPublicationInfo dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_assertion a np:Assertion .
  dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_provenance a np:Provenance .
  dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_assertion {
  miriam-gene:151 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGNbd052a829cec329e7aff89cc4be04a75 sio:SIO_000628 miriam-gene:151 , lld:C0020538 ;
    a sio:SIO_001122 .
}
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_provenance {
  dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_assertion dcterms:description "[Our data suggest that carriers of the DD versus II genotype of the alpha(2B)-adrenoceptor are at increased risk for hypertension. The genotypic effect is most evident when comparing groups corresponding to the upper and lower tails of the blood pressure distribution in the population; however, in nondiabetic hypertensive subjects it is weakly detectable even at the population level.]. 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:14744925 ;
    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:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_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" .
}