@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI> .
@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:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_head {
  this: np:hasAssertion dgn-np:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_assertion;
    np:hasProvenance dgn-np:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_provenance;
    np:hasPublicationInfo dgn-np:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_assertion a np:Assertion .
  
  dgn-np:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_provenance a np:Provenance .
  
  dgn-np:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0023890 a ncit:C7057 .
  
  dgn-gda:DGN32a487121c411e314b960ac3e7c9e6e4 sio:SIO_000628 miriam-gene:4524, lld:C0023890;
    a sio:SIO_001121 .
}

dgn-np:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_provenance {
  dgn-np:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_assertion dcterms:description
      "[We studied thrombophilic genetic factors (TGFs) MTHFR C677TT, PAI1 4G-4G, V Leiden Q506, prothrombin G20210A as risk factors in 94 patients with HCC with and without portal vein thrombosis (PVT), compared with 214 patients with liver cirrhosis (LC) with and without PVT and 94 healthy controls (HC).]. 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:18618228;
    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:NP876536.RADoU15eanecqKR466d0uftvrRomYJdQSb173mYST9ALI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:55+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" .
}