@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM> .
@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:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_head {
  this: np:hasAssertion dgn-np:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_assertion;
    np:hasProvenance dgn-np:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_provenance;
    np:hasPublicationInfo dgn-np:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_assertion a np:Assertion .
  
  dgn-np:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_provenance a np:Provenance .
  
  dgn-np:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_assertion {
  miriam-gene:1493 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGN67b4a8c0c5bf0d0df2d3ccc46ac48257 sio:SIO_000628 miriam-gene:1493, lld:C0004096;
    a sio:SIO_001122 .
}

dgn-np:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_provenance {
  dgn-np:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_assertion dcterms:description
      "[ Our findings suggest that promoter polymorphisms of both CTLA4 and FCER1B are genetic factors that influence total serum IgE levels in patients with asthma. This supports the theory that variance in total serum IgE levels in patients with asthma is determined by mutations in multiple genes, each of which has a relatively small effect on the phenotype.]. 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:11447385;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP46524.RAfZgT0TKc8N_7bVJtGQI2ZqX7K4eacn07i7tbxCFG0nM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}