@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE> .
@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:NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE130_head {
  this: np:hasAssertion dgn-np:NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE130_assertion ;
    np:hasProvenance dgn-np:NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE130_provenance ;
    np:hasPublicationInfo dgn-np:NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE130_provenance a np:Provenance .
  dgn-np:NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE130_assertion {
  miriam-gene:7040 a ncit:C16612 .
  lld:C0002874 a ncit:C7057 .
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dgn-np:NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE130_provenance {
  dgn-np:NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE130_assertion dcterms:description "[To investigate the role of cytokine gene polymorphisms (IL-6/-174, TNF-α/-308, IFN-γ/+874, and TGFβ1/-509) in patients with acquired AA to assess if genotypes associated with higher or lower production were more prevalent than in established control population and to study the possible association of these genotypes with the disease severity.]. 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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  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1138982.RAAOoHLYOkVSujBJQK8czVDMeMgkRkHLBMq7Tvq6-Q_nE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:22+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}