@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q> .
@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:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_head {
  this: np:hasAssertion dgn-np:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_assertion;
    np:hasProvenance dgn-np:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_provenance;
    np:hasPublicationInfo dgn-np:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_assertion a np:Assertion .
  
  dgn-np:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_provenance a np:Provenance .
  
  dgn-np:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_assertion {
  miriam-gene:23495 a ncit:C16612 .
  
  lld:C0009447 a ncit:C7057 .
  
  dgn-gda:DGNa4c6b876b9d175e1a376b9717fdc19b5 sio:SIO_000628 miriam-gene:23495, lld:C0009447;
    a sio:SIO_001122 .
}

dgn-np:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_provenance {
  dgn-np:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_assertion dc:description
      "[Coding variants in tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) have been implicated in common variable immunodeficiency (CVID), but the functional effects of such mutations in relation to the development of the disease have not been entirely established.]. 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:19494827;
    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:NP78113.RARaQkVkDixahgJUt3sJY24OlB9_AJcZKV1GkopEzDR2Q130_publicationInfo {
  this: dc:created "2014-10-02T12:32:38+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}