@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g> .
@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 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:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_head {
  this: np:hasAssertion dgn-np:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_assertion;
    np:hasProvenance dgn-np:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_provenance;
    np:hasPublicationInfo dgn-np:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_assertion a np:Assertion .
  
  dgn-np:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_provenance a np:Provenance .
  
  dgn-np:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_assertion {
  miriam-gene:2147 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGNc54097ef82acb0ffd5fb4a928fd6c34f sio:SIO_000628 miriam-gene:2147, lld:C0038454;
    a sio:SIO_001122 .
}

dgn-np:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_provenance {
  dgn-np:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_assertion dct:description
      "[ Factor II gene 3'-UT G20210A mutant allele is absent in the 99 Chinese Zhuang ethnic patients with ischemic stroke and myocardial infarction and is absent in 106 normal healthy Zhuang people. FII G20210A mutation may not be a major risk factor for thrombogenesis in ethnic Chinese.]. 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:15952132;
    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:NP44533.RAqY0vEaK3rgUXadGEGjQxJ1YIfrPxeqt7kGXxWXEp2-g130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}