@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_head {
   this: np:hasAssertion dgn-np:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_assertion ;
    np:hasProvenance dgn-np:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_provenance ;
    np:hasPublicationInfo dgn-np:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_assertion a np:Assertion .
  dgn-np:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_provenance a np:Provenance .
  dgn-np:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_assertion {
   miriam-gene:23495 a ncit:C16612 .
  lld:C2931161 a ncit:C7057 .
  dgn-gda:DGN06d81b7d224382cc3990ace066ede947 sio:SIO_000628 miriam-gene:23495 , lld:C2931161 ;
    a sio:SIO_001121 .
}
dgn-np:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_provenance {
   dgn-np:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_assertion dcterms:description "[To examine the potential contribution of TNFRSF13B variants to CVID, we have applied an evolutionary approach by sequencing its coding region in 451 individuals belonging to 26 worldwide populations, in addition to controls, patients with CVID and selective IgA deficiency (IgAD) from Italy.]. 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:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP743108.RA20TrBmGImkwYyyJSwP0pWA_avgNq5MTrKN077eUL6n4130_publicationInfo {
   this: dcterms:created "2016-05-13T12:47:22+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}