@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A> .
@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/v4.0.0/void/> .
dgn-np:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_head {
   this: np:hasAssertion dgn-np:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_assertion ;
    np:hasProvenance dgn-np:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_provenance ;
    np:hasPublicationInfo dgn-np:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_assertion a np:Assertion .
  dgn-np:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_provenance a np:Provenance .
  dgn-np:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_assertion {
   miriam-gene:94 a ncit:C16612 .
  lld:C3203102 a ncit:C7057 .
  dgn-gda:DGN91af958e60f4c1c5c3d1e6acbfc03a8c sio:SIO_000628 miriam-gene:94 , lld:C3203102 ;
    a sio:SIO_001121 .
}
dgn-np:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_provenance {
   dgn-np:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_assertion dcterms:description "[Heritable and idiopathic pulmonary arterial hypertension (PAH) are phenotypically identical and associated with mutations in several genes related to transforming growth factor (TGF) beta signaling, including bone morphogenetic protein receptor type 2, activin receptor-like kinase 1, endoglin, and mothers against decapentaplegic 9.]. 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:22474227 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP972521.RA_vJxl1FC4GhZvWXqoN7Fr3SDubZTz0KgFezk9TtAi0A130_publicationInfo {
   this: dcterms:created "2016-05-13T12:49:05+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}