@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE> .
@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:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_head {
  this: np:hasAssertion dgn-np:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_assertion;
    np:hasProvenance dgn-np:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_provenance;
    np:hasPublicationInfo dgn-np:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_assertion a np:Assertion .
  
  dgn-np:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_provenance a np:Provenance .
  
  dgn-np:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_assertion {
  miriam-gene:161835 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGN29289a6dc8b58ad949be2b15284cd42b sio:SIO_000628 miriam-gene:161835, lld:C0004096;
    a sio:SIO_001122 .
}

dgn-np:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_provenance {
  dgn-np:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_assertion dcterms:description
      "[Although our findings did not suggest that SNPs of FSIP1 had an effect on the reversibility of lung function abnormalities in AIA patients, they did show significant evidence of association between the variants in FSIP1 and AIA occurrence among asthmatics in a Korean population.]. 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:20513247;
    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:NP89423.RASYJdRbV5POaKJFbdHpzxyxJCPtPqLoZS63_uwXpe9GE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:44+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" .
}