@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI> .
@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:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_head {
  this: np:hasAssertion dgn-np:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_assertion;
    np:hasProvenance dgn-np:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_provenance;
    np:hasPublicationInfo dgn-np:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_assertion a np:Assertion .
  
  dgn-np:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_provenance a np:Provenance .
  
  dgn-np:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_assertion {
  miriam-gene:659 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_provenance {
  dgn-np:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_assertion dcterms:description
      "[The aim of the present study was to determine if patients with both pulmonary arterial hypertension (PAH), due to pulmonary vascular obstructive disease, and congenital heart defects (CHD), have mutations in the gene encoding bone morphogenetic protein receptor (BMPR)-2.]. 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:15358693;
    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:NP157720.RAp3sWawNdRGHdJeF0I7KXAvTqxyHyvZNhm4nesEV5DPI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:25+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}