@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg> .
@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:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_head {
  this: np:hasAssertion dgn-np:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_assertion ;
    np:hasProvenance dgn-np:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_provenance ;
    np:hasPublicationInfo dgn-np:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_assertion a np:Assertion .
  dgn-np:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_provenance a np:Provenance .
  dgn-np:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_assertion {
  miriam-gene:1590 a ncit:C16612 .
  lld:C0151449 a ncit:C7057 .
  dgn-gda:DGN3ad3b4e2e1394b920978c3f1858d46de sio:SIO_000628 miriam-gene:1590 , lld:C0151449 ;
    a sio:SIO_001121 .
}
dgn-np:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_provenance {
  dgn-np:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_assertion dcterms:description "[Since a deletion of the C4A and CyP21A genes is reported to account for C4AQO in patients with systemic lupus erythematosus (SLE) in Caucasians, we studied the restriction fragment length polymorphism (RFLP) of genomic DNA to determine whether similar deletions of the C4A and CyP21A genes occur in Japanese patients with SS.]. 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:1351942 ;
    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:NP826629.RAOR3eS2DShKKP6_8NqZEFEC2DAJEPlE1wrvRzgqcVdHg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:26+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" .
}