@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1235566.RAiDPPbjGi3BN08pmqVG8ZRSrhJFOXu90YvF2MHAdF9Jw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1235566.RAiDPPbjGi3BN08pmqVG8ZRSrhJFOXu90YvF2MHAdF9Jw130_head {
  this: np:hasAssertion dgn-np:NP1235566.RAiDPPbjGi3BN08pmqVG8ZRSrhJFOXu90YvF2MHAdF9Jw130_assertion ;
    np:hasProvenance dgn-np:NP1235566.RAiDPPbjGi3BN08pmqVG8ZRSrhJFOXu90YvF2MHAdF9Jw130_provenance ;
    np:hasPublicationInfo dgn-np:NP1235566.RAiDPPbjGi3BN08pmqVG8ZRSrhJFOXu90YvF2MHAdF9Jw130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP1235566.RAiDPPbjGi3BN08pmqVG8ZRSrhJFOXu90YvF2MHAdF9Jw130_assertion {
  miriam-gene:282617 a ncit:C16612 .
  lld:C0019163 a ncit:C7057 .
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dgn-np:NP1235566.RAiDPPbjGi3BN08pmqVG8ZRSrhJFOXu90YvF2MHAdF9Jw130_provenance {
  dgn-np:NP1235566.RAiDPPbjGi3BN08pmqVG8ZRSrhJFOXu90YvF2MHAdF9Jw130_assertion dcterms:description "[This was a retrospective cohort study.We genotyped seven SNPs in the following genes, interleukin (IL)-10 (rs1800871 and rs1800872), human leukocyte antigen (HLA)-DPA1 (rs3077), HLA-DPB1 (rs9277535), HLA-DQB2 (rs7453920), HLA-DQB1 (rs2856718), and IL28B (rs8099917), in patients with chronic HBV infection using PCR and sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP1235566.RAiDPPbjGi3BN08pmqVG8ZRSrhJFOXu90YvF2MHAdF9Jw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:06+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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