@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM> .
@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:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_head {
  this: np:hasAssertion dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_assertion ;
    np:hasProvenance dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_provenance ;
    np:hasPublicationInfo dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_assertion a np:Assertion .
  dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_provenance a np:Provenance .
  dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_assertion {
  miriam-gene:1351 a ncit:C16612 .
  lld:C2827470 a ncit:C7057 .
  dgn-gda:DGN823c8bc3627d6666d0f91e403173755a sio:SIO_000628 miriam-gene:1351 , lld:C2827470 ;
    a sio:SIO_001121 .
}
dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_provenance {
  dgn-np:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_assertion dcterms:description "[Thrombophilia was suspected and the relative investigation revealed high levels of factor VIII procoagulant, which is frequent in hemodialysis patients, and resistance to activated protein C. Polymerase chain reaction detected that the patient was heterozygous for factor V Leiden, which is quite common in general population.]. 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:18387172 ;
    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:NP770681.RAit9xdZYwxMk1gmN352WzWWVXmhVGyM1wYbmKS1guEcM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:46+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" .
}