@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk> .
@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:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_head {
  this: np:hasAssertion dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_assertion ;
    np:hasProvenance dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_provenance ;
    np:hasPublicationInfo dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_assertion a np:Assertion .
  dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_provenance a np:Provenance .
  dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_assertion {
  miriam-gene:5554 a ncit:C16612 .
  lld:C0004943 a ncit:C7057 .
  dgn-gda:DGN1dcc206afffeb868c66e0f68182fcad2 sio:SIO_000628 miriam-gene:5554 , lld:C0004943 ;
    a sio:SIO_001121 .
}
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_provenance {
  dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_assertion dcterms:description "[These findings indicate that the H1 haplotype protects Behçet's patients from thrombosis, likely via increased levels of activated protein C, whereas individuals carrying the H3 haplotype seem to be protected from the clinical manifestations associated with Behçet's disease, probably via increased soluble endothelial protein C levels.]. 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:21851971 ;
    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:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:27+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" .
}