@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4> .
@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:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_head {
  this: np:hasAssertion dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_assertion ;
    np:hasProvenance dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_provenance ;
    np:hasPublicationInfo dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_assertion a np:Assertion .
  dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_provenance a np:Provenance .
  dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_assertion {
  miriam-gene:54738 a ncit:C16612 .
  lld:C0004096 a ncit:C7057 .
  dgn-gda:DGNf283a05f114f5a502dd9b0395ff0a4d7 sio:SIO_000628 miriam-gene:54738 , lld:C0004096 ;
    a sio:SIO_001121 .
}
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_provenance {
  dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_assertion dcterms:description "[More interestingly, regression analysis of the decline of forced expiratory volume in one second (FEV(1)) by aspirin provocation revealed that 10 SNPs (P = 0.003-0.04) and four relevant haplotypes (P = 0.002-0.02) were significantly associated with the fall rate of FEV(1) by aspirin provocation, indicating that genetic polymorphisms of EMID2 could cause meaningful deficits in the upper and lower airways among AIA patients.]. 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:21086123 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  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 ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:11+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}