@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ> .
@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:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_head {
  this: np:hasAssertion dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_assertion;
    np:hasProvenance dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_provenance;
    np:hasPublicationInfo dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_assertion a np:Assertion .
  
  dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_provenance a np:Provenance .
  
  dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_assertion {
  miriam-gene:3565 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGNeaa29bbc74382d5ded593624eb30a608 sio:SIO_000628 miriam-gene:3565, lld:C0004096;
    a sio:SIO_001121 .
}

dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_provenance {
  dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_assertion dcterms:description
      "[Because populations of African descent have increased levels of genetic variation compared with other populations, particularly with respect to low frequency or rare variants, we hypothesized that rare variants in the IL4 gene contribute to the development of asthma in African Americans.]. 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:19910025;
    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:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:50+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" .
}