@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU> .
@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:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_head {
  this: np:hasAssertion dgn-np:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_assertion;
    np:hasProvenance dgn-np:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_provenance;
    np:hasPublicationInfo dgn-np:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_assertion a np:Assertion .
  
  dgn-np:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_provenance a np:Provenance .
  
  dgn-np:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_assertion {
  miriam-gene:1666 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_provenance {
  dgn-np:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_assertion dcterms:description
      "[We sought to elucidate the role of genetic variability in the gene encoding the p22(phox) subunit of the NADPH oxidase (CYBA, 16q24.3) in asthma susceptibility by means of an association study of haplotypes based on 3 common single nucleotide polymorphisms (SNPs), -930A/G, 242C/T (H72Y) and 640A/G.]. 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:18716406;
    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:NP542635.RAoZgdJJojWErn8OlzQzx-jnkwE-rM6xqtEQNDeNxrEaU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:27+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: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" .
}