@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg> .
@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:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_head {
  this: np:hasAssertion dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_assertion ;
    np:hasProvenance dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_provenance ;
    np:hasPublicationInfo dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_assertion a np:Assertion .
  dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_provenance a np:Provenance .
  dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_assertion {
  miriam-gene:5660 a ncit:C16612 .
  lld:C0242666 a ncit:C7057 .
  dgn-gda:DGNce44d181f23f906ba150d298ba460eba sio:SIO_000628 miriam-gene:5660 , lld:C0242666 ;
    a sio:SIO_001121 .
}
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_provenance {
  dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_assertion dcterms:description "[Although these traits are present at relatively high prevalence in the population, the magnitude of the increased thrombotic risk associated with these factors is substantially less than that related to inherited deficiency of the natural anticoagulant protein antithrombin, and somewhat less than the elevated risk with protein C and protein S deficiencies.]. 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:11286642 ;
    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:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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" .
}