@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA> .
@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:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_head {
   this: np:hasAssertion dgn-np:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_assertion ;
    np:hasProvenance dgn-np:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_provenance ;
    np:hasPublicationInfo dgn-np:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_assertion a np:Assertion .
  dgn-np:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_provenance a np:Provenance .
  dgn-np:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_assertion {
   miriam-gene:7056 a ncit:C16612 .
  lld:C0007820 a ncit:C7057 .
  dgn-gda:DGNbe1896269d94bcf5e1dc97a0496374d6 sio:SIO_000628 miriam-gene:7056 , lld:C0007820 ;
    a sio:SIO_001122 .
}
dgn-np:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_provenance {
   dgn-np:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_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:NP62549.RA6wBX5y49LdaHnrK6KZmwpg3ccMsYniE4PTYNat3FfGA130_publicationInfo {
   this: dcterms:created "2015-08-25T14:38:14+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" .
}