@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4> .
@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:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_head {
  this: np:hasAssertion dgn-np:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_assertion ;
    np:hasProvenance dgn-np:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_provenance ;
    np:hasPublicationInfo dgn-np:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_assertion a np:Assertion .
  dgn-np:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_provenance a np:Provenance .
  dgn-np:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_assertion {
  miriam-gene:6915 a ncit:C16612 .
  lld:C0004096 a ncit:C7057 .
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    a sio:SIO_001122 .
}
dgn-np:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_provenance {
  dgn-np:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_assertion dcterms:description "[In conclusion, our results suggest that the T924C marker in the TBXA2R gene is associated, in Chinese children, with an increased susceptibility of developing atopic asthma. This marker is also associated with the extent of allergic sensitization to cat, as well as with reduced FEV1 and FVC values.]. 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 ;
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}
dgn-np:NP50809.RAbzvd4AUJU_Nriwkl0873ilq8Kr0psgeajcwSsQzWDa4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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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}