@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU> .
@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:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_head {
  this: np:hasAssertion dgn-np:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_assertion;
    np:hasProvenance dgn-np:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_provenance;
    np:hasPublicationInfo dgn-np:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_assertion a np:Assertion .
  
  dgn-np:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_provenance a np:Provenance .
  
  dgn-np:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_assertion {
  miriam-gene:657 a ncit:C16612 .
  
  lld:C0152171 a ncit:C7057 .
  
  dgn-gda:DGN79ef5df89af1ae299c9584d9e579dc14 sio:SIO_000628 miriam-gene:657, lld:C0152171;
    a sio:SIO_001121 .
}

dgn-np:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_provenance {
  dgn-np:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_assertion dcterms:description
      "[This study screened for mutations in endoglin, SMAD1, SMAD2, SMAD3, SMAD4, SMAD5, SMAD6, SMAD7, bone morphogenetic protein receptor type 1A (BMPR1A) and bone morphogenetic protein receptor type 1B (BMPR1B) genes in 43 IPAH patients who had no mutations in BMPR2, ALK1 and SMAD8.]. 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:22374147;
    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:NP539443.RADUt_ExARBUFOfQYp3OVqHaoMbsZc2lyGsbKiCk6mqZU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:25+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>,
      <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" .
}