@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ> .
@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:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_head {
  this: np:hasAssertion dgn-np:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_assertion;
    np:hasProvenance dgn-np:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_provenance;
    np:hasPublicationInfo dgn-np:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_assertion a np:Assertion .
  
  dgn-np:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_provenance a np:Provenance .
  
  dgn-np:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_assertion {
  miriam-gene:3594 a ncit:C16612 .
  
  lld:C0026918 a ncit:C7057 .
  
  dgn-gda:DGNf1a036e0e3c5665cc23ac0a6836f16aa sio:SIO_000628 miriam-gene:3594, lld:C0026918;
    a sio:SIO_001121 .
}

dgn-np:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_provenance {
  dgn-np:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_assertion dcterms:description
      "[Even though the IgA deficiency in itself does not predispose to mycobacterial disease, the lack of secreted IgA may have disturbed the intestinal homoeostasis and increased the susceptibility to the low-virulent mycobacterium that the patient was not able to clear because of his IL12R deficiency.]. 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:21812800;
    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:NP629620.RASixADc8HBcL4jmFQqL44p_1IUrapS_P42V8Wwwe1pGQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:20+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" .
}