@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44163.RAeLr-LjjdgNygzyjIntjCnUplg4ZPB_jjYaznov3jy5I> .
@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:NP44163.RAeLr-LjjdgNygzyjIntjCnUplg4ZPB_jjYaznov3jy5I130_head {
  this: np:hasAssertion dgn-np:NP44163.RAeLr-LjjdgNygzyjIntjCnUplg4ZPB_jjYaznov3jy5I130_assertion ;
    np:hasProvenance dgn-np:NP44163.RAeLr-LjjdgNygzyjIntjCnUplg4ZPB_jjYaznov3jy5I130_provenance ;
    np:hasPublicationInfo dgn-np:NP44163.RAeLr-LjjdgNygzyjIntjCnUplg4ZPB_jjYaznov3jy5I130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP44163.RAeLr-LjjdgNygzyjIntjCnUplg4ZPB_jjYaznov3jy5I130_assertion {
  miriam-gene:2207 a ncit:C16612 .
  lld:C0027726 a ncit:C7057 .
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dgn-np:NP44163.RAeLr-LjjdgNygzyjIntjCnUplg4ZPB_jjYaznov3jy5I130_provenance {
  dgn-np:NP44163.RAeLr-LjjdgNygzyjIntjCnUplg4ZPB_jjYaznov3jy5I130_assertion dcterms:description "[We conclude that  polymorphisms in the IL4 receptor, the high-affinity IgE receptor and IL13 do not seem to predict the clinical course of NS, despite the fact that serum IgE elevations are more frequent in patients with NS than in normal control subjects. The investigated polymorphisms may contribute to the IgE switch in patients with NS.]. 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:gad-20130706 ;
    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:NP44163.RAeLr-LjjdgNygzyjIntjCnUplg4ZPB_jjYaznov3jy5I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}