@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY> .
@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:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_head {
  this: np:hasAssertion dgn-np:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_assertion;
    np:hasProvenance dgn-np:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_provenance;
    np:hasPublicationInfo dgn-np:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_assertion a np:Assertion .
  
  dgn-np:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_provenance a np:Provenance .
  
  dgn-np:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_assertion {
  miriam-gene:3567 a ncit:C16612 .
  
  lld:C0375023 a ncit:C7057 .
  
  dgn-gda:DGNaac196b363cb5da7aca2c6d787f69c60 sio:SIO_000628 miriam-gene:3567, lld:C0375023;
    a sio:SIO_001121 .
}

dgn-np:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_provenance {
  dgn-np:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_assertion dcterms:description
      "[To investigate the genetic basis for RSV disease severity, linked variants of 3 Th2 cytokine genes, IL4, IL13, and IL5 (which are clustered on chromosome 5q31.1) were characterized in 105 children who were hospitalized with severe RSV infection and 315 Korean control subjects in a pilot study.]. 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:12402189;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP936689.RAhVdKyr4kjiIms1Ra7-7a1EJ53EVjz4Vx5P6OnwLjCAY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:34+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" .
}