@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo> .
@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:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_head {
  this: np:hasAssertion dgn-np:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_assertion ;
    np:hasProvenance dgn-np:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_provenance ;
    np:hasPublicationInfo dgn-np:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_assertion a np:Assertion .
  dgn-np:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_provenance a np:Provenance .
  dgn-np:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_assertion {
  miriam-gene:81622 a ncit:C16612 .
  lld:C0276226 a ncit:C7057 .
  dgn-gda:DGN4e86a75b0abd55648ccfe9b7e5b92474 sio:SIO_000628 miriam-gene:81622 , lld:C0276226 ;
    a sio:SIO_001121 .
}
dgn-np:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_provenance {
  dgn-np:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_assertion dcterms:description "[Autosomal recessive IRAK-4 and myeloid differentiation factor 88 deficiencies were reported in 2003 and 2008, respectively, conferring predisposition to pyogenic bacterial infections, and autosomal recessive UNC93B1 and autosomal dominant TLR3 deficiencies were reported in 2006 and 2007, respectively, conferring predisposition to herpes simplex encephalitis.]. 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:19430930 ;
    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:NP282897.RA2F7BztKwHVOMTZOBO_rzbki7lsK6HXpNfoFsOvK0GIo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:39+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" .
}