@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI> .
@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:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_head {
  this: np:hasAssertion dgn-np:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_assertion ;
    np:hasProvenance dgn-np:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_provenance ;
    np:hasPublicationInfo dgn-np:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_assertion a np:Assertion .
  dgn-np:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_provenance a np:Provenance .
  dgn-np:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_assertion {
  miriam-gene:5554 a ncit:C16612 .
  lld:C0038454 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_provenance {
  dgn-np:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_assertion dcterms:description "[We assessed the occurrence of several prothrombotic states (factor V Leiden, prothrombin G20210A, deficiencies in protein S, protein C and antithrombin, lupus anticoagulant, anticardiolipin antibodies, elevated factor VIII, resistance to activated protein C) and classical risk factors for venous thrombosis in 57 adult patients with cryptogenic stroke and patent foramen ovale and in 104 matched controls.]. 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:12695749 ;
    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:NP415874.RAB53i5OX5hGF2XDW65H-y2FacuhChXwz6V05rnR2axaI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:07+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}