@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE> .
@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:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_head {
  this: np:hasAssertion dgn-np:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_assertion;
    np:hasProvenance dgn-np:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_provenance;
    np:hasPublicationInfo dgn-np:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_assertion a np:Assertion .
  
  dgn-np:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_provenance a np:Provenance .
  
  dgn-np:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_assertion {
  miriam-gene:2260 a ncit:C16612 .
  
  lld:C0013595 a ncit:C7057 .
  
  dgn-gda:DGN23132b5be3879bda337e81d4f81728a3 sio:SIO_000628 miriam-gene:2260, lld:C0013595;
    a sio:SIO_001121 .
}

dgn-np:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_provenance {
  dgn-np:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_assertion dcterms:description
      "[Our comprehensive screening suggested that population-specific FLG mutations may be a significant predisposing factor for hay fever (odds ratio = 2.01 [95% CI: 1.027-3.936, P &lt; 0.05]), although the sample sizes of this study were too small for reliable subphenotype analysis on the association between FLG mutations and hay fever in the eczema patients and the noneczema individuals, and it is not clear whether the association between FLG mutations and hay fever is due to the close association between FLG mutations and hay fever patients with eczema.]. 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:24467288;
    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:NP1149103.RAm3Ea8M3Rm2huRRaUz-5t4H7d8XoJeYCCiYosqG0eZtE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:27+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" .
}