@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE> .
@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:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_head {
  this: np:hasAssertion dgn-np:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_assertion;
    np:hasProvenance dgn-np:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_provenance;
    np:hasPublicationInfo dgn-np:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_assertion a np:Assertion .
  
  dgn-np:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_provenance a np:Provenance .
  
  dgn-np:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C1861172 a ncit:C7057 .
  
  dgn-gda:DGN98059f9443d8d767cfd521c6b767f5ba sio:SIO_000628 miriam-gene:2153, lld:C1861172;
    a sio:SIO_001122 .
}

dgn-np:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_provenance {
  dgn-np:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_assertion dcterms:description
      "[Carriership of FV Leiden or FII A20210 mutations identifies an at-risk condition for venous thrombosis in the lower extremities, SVT or CVT. In patients with SVT, screening for the JAK2 V617F mutation may be useful in recognising patients who should be carefully observed for the subsequent development of overt MPD. Thus, genetic tests may play a different ro]. 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:17307838;
    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:NP44435.RAfaqmtK2bOhFVNOFW2B9eulxAQXLuvNBPIfK62uAR-rE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}