@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y> .
@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:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_head {
  this: np:hasAssertion dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_assertion;
    np:hasProvenance dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_provenance;
    np:hasPublicationInfo dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_assertion a np:Assertion .
  
  dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_provenance a np:Provenance .
  
  dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_assertion {
  miriam-gene:5277 a ncit:C16612 .
  
  lld:C0002878 a ncit:C7057 .
  
  dgn-gda:DGN16cd40a435bc52bae95bad7564d374a5 sio:SIO_000628 miriam-gene:5277, lld:C0002878;
    a sio:SIO_001121 .
}

dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_provenance {
  dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_assertion dcterms:description
      "[The development of pulmonary arterial hypertension (PAH) is the leading cause of mortality in patients with thalassemia and sickle cell anemia and was reported to occur in hemolytic anemias such as hereditary stomatocytosis, and paroxysmal nocturnal hemoglobinuria.]. 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:17356397;
    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:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:11+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" .
}