@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k> .
@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:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_head {
  this: np:hasAssertion dgn-np:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_assertion ;
    np:hasProvenance dgn-np:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_provenance ;
    np:hasPublicationInfo dgn-np:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_assertion a np:Assertion .
  dgn-np:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_provenance a np:Provenance .
  dgn-np:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_assertion {
  miriam-gene:3593 a ncit:C16612 .
  lld:C0004096 a ncit:C7057 .
  dgn-gda:DGNfd7163bdc7d29fbd0895556e59dd45c6 sio:SIO_000628 miriam-gene:3593 , lld:C0004096 ;
    a sio:SIO_001122 .
}
dgn-np:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_provenance {
  dgn-np:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_assertion dcterms:description "[ In this long-term study of asthmatic subjects with comprehensive data on asthma severity, we found no evidence to support the presence of a heterozygote effect of the IL12B promoter polymorphism on the level of asthma in early childhood or adulthood. The polymorphism was also not associated with asthma susceptibility, but the CTCTAA allele may have been associated with elevated serum IgE levels in male subjects and reduced pulmonary function in female subjects in early childhood.]. 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 .
  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:NP56642.RAcSb4H5Ch3PmtowULh4F_WNHf6qbS8NLzosDPwCXCl8k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
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}