@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45224.RALuaVmyP7IjR2BAPO8emGa-S5Ie4EE-u2NWRYQwBlgQs> .
@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:NP45224.RALuaVmyP7IjR2BAPO8emGa-S5Ie4EE-u2NWRYQwBlgQs130_head {
  this: np:hasAssertion dgn-np:NP45224.RALuaVmyP7IjR2BAPO8emGa-S5Ie4EE-u2NWRYQwBlgQs130_assertion ;
    np:hasProvenance dgn-np:NP45224.RALuaVmyP7IjR2BAPO8emGa-S5Ie4EE-u2NWRYQwBlgQs130_provenance ;
    np:hasPublicationInfo dgn-np:NP45224.RALuaVmyP7IjR2BAPO8emGa-S5Ie4EE-u2NWRYQwBlgQs130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP45224.RALuaVmyP7IjR2BAPO8emGa-S5Ie4EE-u2NWRYQwBlgQs130_provenance a np:Provenance .
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}
dgn-np:NP45224.RALuaVmyP7IjR2BAPO8emGa-S5Ie4EE-u2NWRYQwBlgQs130_assertion {
  miriam-gene:1906 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGN7fc253c3f72d9ee47c4fb2ce49ebcd25 sio:SIO_000628 miriam-gene:1906 , lld:C0020538 ;
    a sio:SIO_001122 .
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dgn-np:NP45224.RALuaVmyP7IjR2BAPO8emGa-S5Ie4EE-u2NWRYQwBlgQs130_provenance {
  dgn-np:NP45224.RALuaVmyP7IjR2BAPO8emGa-S5Ie4EE-u2NWRYQwBlgQs130_assertion dcterms:description "[Our transient expression study indicates that the Lys198Asn polymorphism may not directly affect ET-1 and big ET-1 production. Another variant in the EDN1 gene in linkage disequilibrium with the Lys198Asn polymorphism may be responsible for the association with BP, or the interaction between the EDN1 Lys198Asn polymorphism and other factors such as obesity may be involved in the mechanisms elevating BP in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
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  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:NP45224.RALuaVmyP7IjR2BAPO8emGa-S5Ie4EE-u2NWRYQwBlgQs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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