@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw> .
@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:NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw130_head {
  this: np:hasAssertion dgn-np:NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw130_assertion ;
    np:hasProvenance dgn-np:NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw130_provenance ;
    np:hasPublicationInfo dgn-np:NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw130_publicationInfo ;
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  dgn-np:NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw130_provenance a np:Provenance .
  dgn-np:NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw130_assertion {
  miriam-gene:4758 a ncit:C16612 .
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dgn-np:NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw130_provenance {
  dgn-np:NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw130_assertion dcterms:description "[In the present study, we designed an association study to investigate polymorphisms of two important genes, ST6GALNAC2 and NEU1, which are involved in the sialylation of the IgA1 molecule, in the susceptibility to IgAN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    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:NP788408.RA19FjcH-xcw6XihdouLQIeaUcJkSkzC3192olhKVHguw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:01+02:00"^^xsd:dateTime ;
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    dcterms:rightsHolder dgn-void:IBIGroup ;
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