@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao> .
@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:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_head {
  this: np:hasAssertion dgn-np:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_assertion;
    np:hasProvenance dgn-np:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_provenance;
    np:hasPublicationInfo dgn-np:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_assertion a np:Assertion .
  
  dgn-np:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_provenance a np:Provenance .
  
  dgn-np:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_assertion {
  miriam-gene:3958 a ncit:C16612 .
  
  lld:C0948008 a ncit:C7057 .
  
  dgn-gda:DGNfb68034d68dfa57034dc60f41459355d sio:SIO_000628 miriam-gene:3958, lld:C0948008;
    a sio:SIO_001121 .
}

dgn-np:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_provenance {
  dgn-np:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_assertion dcterms:description
      "[In the present study, we examined whether the LGALS2 3279TT homozygote variant alone can influence the prevalence of ischaemic stroke, and whether it can interact somehow with the disadvantageous LTA 252GG homozygote variant.]. 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:19013708;
    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:NP661863.RABjrYUmXA76L7e3LhrlCKY1I51epDy1aDRz57ir-eeao130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:40+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" .
}