@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c> .
@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:NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c130_head {
  this: np:hasAssertion dgn-np:NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c130_assertion ;
    np:hasProvenance dgn-np:NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c130_provenance ;
    np:hasPublicationInfo dgn-np:NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c130_provenance a np:Provenance .
  dgn-np:NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c130_assertion {
  miriam-gene:3769 a ncit:C16612 .
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dgn-np:NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c130_provenance {
  dgn-np:NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c130_assertion dcterms:description "[The aim of the study was to investigate the association between the FXIII Val34Leu polymorphism and the risk of ischemic stroke due to small vessel disease (SVD) or the risk of primary intracerebral hemorrhage (PICH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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 ;
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}
dgn-np:NP549442.RAASni-kwWexTnB6o8mV3NiIFIMrPG-usDUU2CVTSbf7c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:31+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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