@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk> .
@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:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_head {
  this: np:hasAssertion dgn-np:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_assertion ;
    np:hasProvenance dgn-np:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_provenance ;
    np:hasPublicationInfo dgn-np:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_assertion a np:Assertion .
  dgn-np:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_provenance a np:Provenance .
  dgn-np:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_assertion {
  miriam-gene:959 a ncit:C16612 .
  lld:C0272236 a ncit:C7057 .
  dgn-gda:DGNd4fcd9de18f3ccc8379ee36f8eaeb6ae sio:SIO_000628 miriam-gene:959 , lld:C0272236 ;
    a sio:SIO_001121 .
}
dgn-np:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_provenance {
  dgn-np:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_assertion dcterms:description "[The in vivo critical role of CD40-CD154 interaction on B-cell differentiation and isotype switching is provided by the discovery that mutations in either CD40 or CD154 gene cause the hyper IgM syndrome, termed HIGM3 or HIGM1, respectively, characterized by very low levels of serum IgG, IgA, and IgE, with normal or elevated IgM, associated with a defective germinal center formation.]. 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:15661021 ;
    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:NP583809.RAC_CVVs6luKuZZW-gBNKQk1FeZVHOp3nxt16ud0TLpEk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:51+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" .
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}