@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU> .
@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:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_head {
  this: np:hasAssertion dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_assertion ;
    np:hasProvenance dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_provenance ;
    np:hasPublicationInfo dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_assertion a np:Assertion .
  dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_provenance a np:Provenance .
  dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_assertion {
  miriam-gene:57379 a ncit:C16612 .
  lld:C0002871 a ncit:C7057 .
  dgn-gda:DGNcc04f904add38e4a6e145779c271150b sio:SIO_000628 miriam-gene:57379 , lld:C0002871 ;
    a sio:SIO_001121 .
}
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_provenance {
  dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_assertion dcterms:description "[In the group of patients with hyper IgM syndrome, the patients with mutations in AID were older at the age of diagnosis, were more likely to have positive isohemagglutinins, and were less likely to have anemia, neutropenia, or thrombocytopenia.]. 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:11112359 ;
    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:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:25+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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}