@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ> .
@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:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_head {
  this: np:hasAssertion dgn-np:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_assertion;
    np:hasProvenance dgn-np:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_provenance;
    np:hasPublicationInfo dgn-np:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_assertion a np:Assertion .
  
  dgn-np:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_provenance a np:Provenance .
  
  dgn-np:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_assertion {
  miriam-gene:326 a ncit:C16612 .
  
  lld:C0006845 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_provenance {
  dgn-np:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_assertion dcterms:description
      "[These observations suggest that iNKT cell deficiency is part of the CMC disease phenotype irrespective of the presence of AIRE gene mutations but does not appear to confer susceptibility to chronic Candida infections.]. 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:20923687;
    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:NP277710.RA3ruZmAyn48DWa49cNCqy4JBDaXNdGpkGD03OV7Ru-RQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:36+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}