@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE> .
@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 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:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_head {
  this: np:hasAssertion dgn-np:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_assertion;
    np:hasProvenance dgn-np:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_provenance;
    np:hasPublicationInfo dgn-np:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_assertion a np:Assertion .
  
  dgn-np:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_provenance a np:Provenance .
  
  dgn-np:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_assertion {
  miriam-gene:3567 a ncit:C16612 .
  
  lld:C0027430 a ncit:C7057 .
  
  dgn-gda:DGNe54f6361a518773a9c6aa09098de92aa sio:SIO_000628 miriam-gene:3567, lld:C0027430;
    a sio:SIO_001122 .
}

dgn-np:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_provenance {
  dgn-np:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_assertion dct:description
      "[We recruited 284 patients with NP in four participating hospitals in Belgium and 427 healthy controls, and genotyped 10 SNPs affecting eosinophilia (rs1420101 in IL1RL1, rs12619285 in IKZF2, rs4431128 in GATA2, rs4143832 in IL5, rs3184504 in SH2B3, rs2416257 in WDR36, rs2269426 in MHC, rs9494145 in MYB, rs748065 in GFRA2, and rs3939286 in IL33) using MALDI-TOF.]. 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:19860791;
    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:NP72054.RAXEeLI-w8t0eKpCIyBAo1m-ftCyHCMlEGJ45i4X_MvsE130_publicationInfo {
  this: dct:created "2014-10-02T12:32:35+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}