@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o> .
@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:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_head {
   this: np:hasAssertion dgn-np:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_assertion ;
    np:hasProvenance dgn-np:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_provenance ;
    np:hasPublicationInfo dgn-np:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_assertion a np:Assertion .
  dgn-np:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_provenance a np:Provenance .
  dgn-np:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_assertion {
   miriam-gene:6401 a ncit:C16612 .
  lld:C0007820 a ncit:C7057 .
  dgn-gda:DGN7e916b980bf11ed859bbcb9f3610a856 sio:SIO_000628 miriam-gene:6401 , lld:C0007820 ;
    a sio:SIO_001122 .
}
dgn-np:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_provenance {
   dgn-np:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_assertion dcterms:description "[It is expected that this study will yield important information on genetic risk factors for the cerebrovascular disease phenotype in SCD by clarifying the role of candidate genes in the development of high TCD. The genomewide screen for a large number of ]. 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:12871600 ;
    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:NP64884.RAD2Ea8tGk3D5AShMAuz83DVK079w_oK5d8v7rz6Fbq9o130_publicationInfo {
   this: dcterms:created "2015-08-25T14:38:15+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" .
}