@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs> .
@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:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_head {
  this: np:hasAssertion dgn-np:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_assertion ;
    np:hasProvenance dgn-np:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_provenance ;
    np:hasPublicationInfo dgn-np:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_assertion a np:Assertion .
  dgn-np:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_provenance a np:Provenance .
  dgn-np:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_assertion {
  miriam-gene:5340 a ncit:C16612 .
  lld:C0600433 a ncit:C7057 .
  dgn-gda:DGN8edfe9aee569679f4730e65abf174f61 sio:SIO_000628 miriam-gene:5340 , lld:C0600433 ;
    a sio:SIO_001121 .
}
dgn-np:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_provenance {
  dgn-np:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_assertion dcterms:description "[Here we report a neonate with bilateral RVT and adrenal haemorrhage associated with a heterozygous mutation of the gene encoding for clotting factor V, resulting in resistance to activated protein C. Vigorous thrombolytic therapy with urokinase followed by recombinant tissue plasminogen activator dissolved the thrombus in the inferior vena cava and restored perfusion of both kidneys.]. 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:8971893 ;
    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:NP535982.RA1Y6JsSE5WP-BekoBSS4PCV8vc_MX1lmls8dFlXyFoQs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:23+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" .
}