@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g> .
@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:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_head {
  this: np:hasAssertion dgn-np:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_assertion;
    np:hasProvenance dgn-np:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_provenance;
    np:hasPublicationInfo dgn-np:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_assertion a np:Assertion .
  
  dgn-np:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_provenance a np:Provenance .
  
  dgn-np:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_assertion {
  miriam-gene:2022 a ncit:C16612 .
  
  lld:C0152171 a ncit:C7057 .
  
  dgn-gda:DGNb91096c05cbcb51c3ec608f998b623a9 sio:SIO_000628 miriam-gene:2022, lld:C0152171;
    a sio:SIO_001121 .
}

dgn-np:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_provenance {
  dgn-np:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_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-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:NP784662.RAmNeAGvL0F-74erkMUHqiHfffX8AY9LkaflQ8pIJQt7g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:55+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" .
}