@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0> .
@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:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_head {
  this: np:hasAssertion dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_assertion;
    np:hasProvenance dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_provenance;
    np:hasPublicationInfo dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_assertion a np:Assertion .
  
  dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_provenance a np:Provenance .
  
  dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_assertion {
  miriam-gene:1284 a ncit:C16612 .
  
  lld:C0232197 a ncit:C7057 .
  
  dgn-gda:DGN6f0635328b407622397d0c028b0326f3 sio:SIO_000628 miriam-gene:1284, lld:C0232197;
    a sio:SIO_001121 .
}

dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_provenance {
  dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_assertion dcterms:description
      "[Even if patients undergo screening with MRI as well as genotyping, currently available data on the role of MRI on risk of ICH and warfarin ICH do not support use of these tests for withholding anticoagulation in patients with atrial fibrillation.]. 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:18845797;
    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:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:07+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" .
}