@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_head {
  this: np:hasAssertion dgn-np:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_assertion ;
    np:hasProvenance dgn-np:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_provenance ;
    np:hasPublicationInfo dgn-np:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_assertion a np:Assertion .
  dgn-np:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_provenance a np:Provenance .
  dgn-np:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_assertion {
  miriam-gene:7432 a ncit:C16612 .
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}
dgn-np:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_provenance {
  dgn-np:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_assertion dcterms:description "[To explore the underlying molecular mechanisms in this model, it was examined whether absence of the VIP gene might alter the expression of additional genes involved in the pathogenesis of PAH, as single-gene deletions, in the absence of hypoxia, rarely result in significant pulmonary vascular remodelling.]. 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:18166594 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP774966.RAvEOOUsKGYY72kGxt7g6y-FZHulBWmSN0OkBMhBAt9zM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:28+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v3.0.0.0" .
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}