@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds> .
@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:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_head {
  this: np:hasAssertion dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_assertion;
    np:hasProvenance dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_provenance;
    np:hasPublicationInfo dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_assertion a np:Assertion .
  
  dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_provenance a np:Provenance .
  
  dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGNe74d7d812148c32d2e386923dc382289 sio:SIO_000628 miriam-gene:3133, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_provenance {
  dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_assertion dcterms:description
      "[Major histocompatibility complex (MHC) class II combined immunodeficiency (CID), also known as type II bare lymphocyte syndrome, is an autosomal recessive genetic disorder characterized by the complete lack of expression of MHC class II antigens.]. 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:8642248;
    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:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:45+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" .
}