@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0> .
@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:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_head {
  this: np:hasAssertion dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_assertion ;
    np:hasProvenance dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_provenance ;
    np:hasPublicationInfo dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_assertion a np:Assertion .
  dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_provenance a np:Provenance .
  dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_assertion {
  miriam-gene:1906 a ncit:C16612 .
  lld:C0040038 a ncit:C7057 .
  dgn-gda:DGN1a5d9d3d487cdcbbd709c95c86201035 sio:SIO_000628 miriam-gene:1906 , lld:C0040038 ;
    a sio:SIO_001121 .
}
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_provenance {
  dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_assertion dcterms:description "[In order to investigate the possible association of the -231 G > A polymorphism in the endothelin-1 type A receptor gene (EDNRA), previously shown to be associated with other conditions characterized by vasospasm, we examined 77 Caucasian preeclamptic women and 67 matched controls including normotensive subjects without history of thromboembolic event, abnormalities in blood pressure, proteinuria, edema and preeclampsia.]. 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:17437213 ;
    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:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:01+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" .
}