@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y> .
@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:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_head {
  this: np:hasAssertion dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_assertion;
    np:hasProvenance dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_provenance;
    np:hasPublicationInfo dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_assertion a np:Assertion .
  
  dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_provenance a np:Provenance .
  
  dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_assertion {
  miriam-gene:23495 a ncit:C16612 .
  
  lld:C0272238 a ncit:C7057 .
  
  dgn-gda:DGNe02e864859b55a84f7ef9f14d0865cdf sio:SIO_000628 miriam-gene:23495, lld:C0272238;
    a sio:SIO_001121 .
}

dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_provenance {
  dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_assertion dcterms:description
      "[Considering that TNFRSF13B/TACI is very polymorphic and the frequency of its alterations may be different in various ethnic groups, we analyzed their prevalence in 47 Greek patients with antibody deficiencies, including CVID (16 patients), IgAD (16 patients), selective IgG4D (11 patients), and transient hypogammaglobulinemia of infancy (4 patients).]. 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:21547394;
    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:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:52+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" .
}