@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_head {
   this: np:hasAssertion dgn-np:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_assertion ;
    np:hasProvenance dgn-np:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_provenance ;
    np:hasPublicationInfo dgn-np:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_assertion a np:Assertion .
  dgn-np:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_provenance a np:Provenance .
  dgn-np:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_assertion {
   miriam-gene:2212 a ncit:C16612 .
  lld:C0038454 a ncit:C7057 .
  dgn-gda:DGNfc7eb1d202cbffdf3bea0da4c28239d6 sio:SIO_000628 miriam-gene:2212 , lld:C0038454 ;
    a sio:SIO_001122 .
}
dgn-np:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_provenance {
   dgn-np:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_assertion dcterms:description "[These results suggest that IL1RN*1/IL1RN*2 genotype in greater Yin person might be associated with increased risk of ischemic stroke, and rs7535475 of FCGR2A might be associated with decreased risk of ischemic stroke. Furthermore, this relationship could ]. 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:20034444 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP140004.RAjP7T2M36ApWnMrMNzMWncNdG5sUvnwRb61LfuPfLozI130_publicationInfo {
   this: dcterms:created "2015-08-25T14:38:58+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}