@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA> .
@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:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_head {
  this: np:hasAssertion dgn-np:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_assertion ;
    np:hasProvenance dgn-np:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_provenance ;
    np:hasPublicationInfo dgn-np:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_assertion a np:Assertion .
  dgn-np:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_provenance a np:Provenance .
  dgn-np:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  lld:C0017661 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_provenance {
  dgn-np:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_assertion dcterms:description "[We performed an association study of patients with IgA nephropathy and matching control subjects to test whether the G38A polymorphism in the uteroglobin gene, the C2093T polymorphism in the megsin gene, or the angiotensin-converting enzyme (ACE) insertion/deletion polymorphism is associated with IgA nephropathy or rate of disease progression in patients with IgA nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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}
dgn-np:NP343119.RA0YDsxZwIJ8v_bwxqxmk0hXNxRBYfybfoC6ohhW9S4kA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:22+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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}