@prefix orcid: <http://orcid.org/> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE> .
@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 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:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_head {
   this: np:hasAssertion dgn-np:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_assertion ;
    np:hasProvenance dgn-np:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_provenance ;
    np:hasPublicationInfo dgn-np:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_assertion a np:Assertion .
  dgn-np:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_provenance a np:Provenance .
  dgn-np:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_assertion {
   miriam-gene:695 a ncit:C16612 .
  lld:C0221026 a ncit:C7057 .
  dgn-gda:DGNe3ce95c65773eb0a97e819785cd96390 sio:SIO_000628 miriam-gene:695 , lld:C0221026 ;
    a sio:SIO_001122 .
}
dgn-np:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_provenance {
   dgn-np:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_assertion dc:description "[Excluding the patients in whom the marked decrease in B cell numbers characteristic of XLA could not be confirmed by immunofluorescence studies, mutations in Btk were identified in 43 of 46 patients with presumed sporadic XLA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_curated ;
    sio:SIO_000772 miriam-pubmed:9545398 ;
    prov:wasDerivedFrom dgn-void:uniprot-2016 ;
    prov:wasGeneratedBy eco:ECO_0000218 .
  dgn-void:source_evidence_curated a eco:ECO_0000205 ;
    rdfs:comment "Gene-disease associations manually curated."@en ;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  dgn-void:uniprot-2016 pav:importedOn "2016-01-25"^^xsd:date .
}
dgn-np:NP9709.RAk8c4PZBH11UhIsbg82wvmXWb3S0qmo-nkphIkDvJ-BE130_publicationInfo {
   this: dc:created "2016-05-13T12:41:54+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:disgenetv3.0rdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}