@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI> .
@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:NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI130_head {
  this: np:hasAssertion dgn-np:NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI130_assertion ;
    np:hasProvenance dgn-np:NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI130_provenance ;
    np:hasPublicationInfo dgn-np:NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI130_provenance a np:Provenance .
  dgn-np:NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI130_assertion {
  miriam-gene:1791 a ncit:C16612 .
  lld:C0017661 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI130_provenance {
  dgn-np:NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI130_assertion dcterms:description "[Alternatively, if the case-control study design is employed to identify associations between particular candidate genes or markers and the development of IgAN, spurious associations caused by the effects of population stratification should be ruled out by confirming the findings using powerful and sensitive family-based methodologies such as the transmission/dysequilibrium test (TDT).]. 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:10792601 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP364392.RA3KKMTWxfXbmFt15y5cJWmKdPRVmYXqKF2G0IyF_6EXI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:33+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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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}