@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco> .
@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:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_head {
  this: np:hasAssertion dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_assertion;
    np:hasProvenance dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_provenance;
    np:hasPublicationInfo dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_assertion a np:Assertion .
  
  dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_provenance a np:Provenance .
  
  dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_assertion {
  miriam-gene:1234 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGNf8fb45598004608b5176d05887da7637 sio:SIO_000628 miriam-gene:1234, lld:C0004096;
    a sio:SIO_001122 .
}

dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_provenance {
  dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_assertion dct:description
      "[ In a population with a high allelic frequency for the CCR5Delta32 mutation, a significant protection against childhood asthma is evident which is independent of atopy. This protection is lost in the transition between childhood and early adulthood. The contribution of different genetic candidates to the expression of asthma may change with advancing maturity and confound the interpretation of association and linkage studies unless age is taken into account.]. 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:12612298;
    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:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+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" .
}