@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI> .
@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:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_head {
  this: np:hasAssertion dgn-np:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_assertion;
    np:hasProvenance dgn-np:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_provenance;
    np:hasPublicationInfo dgn-np:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_assertion a np:Assertion .
  
  dgn-np:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_provenance a np:Provenance .
  
  dgn-np:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_assertion {
  miriam-gene:2147 a ncit:C16612 .
  
  lld:C0151945 a ncit:C7057 .
  
  dgn-gda:DGN8fba7ed538a3a33bc0ab6a736ff31809 sio:SIO_000628 miriam-gene:2147, lld:C0151945;
    a sio:SIO_001122 .
}

dgn-np:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_provenance {
  dgn-np:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_assertion dcterms:description
      "[ In this large series of CVT patients, a positive association with established thrombophilic risk factors FVL and especially the PT G20210A mutation was confirmed. In contrast, our study found no significant association of CVT with SNPs of the TAFI and the PZ genes. Other than testing for FVL and the PT G20210A mutation, exploration of these potential thrombophilic variants seems to be of limited value in the investigation of CVT.]. 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:16155788;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP62637.RAN-MJf0BQW6Tfz50E9HNhL1_ckKoT8DYgr13fT8WVQNI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}