@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0> .
@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:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_head {
  this: np:hasAssertion dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_assertion;
    np:hasProvenance dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_provenance;
    np:hasPublicationInfo dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_assertion a np:Assertion .
  
  dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_provenance a np:Provenance .
  
  dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN84832cf3dc340248ed52b94c95e1d94e sio:SIO_000628 miriam-gene:1636, lld:C0024141;
    a sio:SIO_001122 .
}

dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_provenance {
  dgn-np:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_assertion dcterms:description
      "[Taken together, the I/D polymorphisms of ACE gene did not affect susceptibility of SLE, lupus nephritis and the vascular manifestations, including Raynaud's phenomenon, in Korean SLE patients, although the DD genotype was negatively associated with Raynaud's phenomenon among SLE patients.]. 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:12043886;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP49556.RAD0sB1AeBU1vU46rqs-S9XSm2CxrjvBYbyrvNl3I_uD0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}