@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc> .
@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:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_head {
  this: np:hasAssertion dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_assertion ;
    np:hasProvenance dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_provenance ;
    np:hasPublicationInfo dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_assertion a np:Assertion .
  dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_provenance a np:Provenance .
  dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  lld:C0272236 a ncit:C7057 .
  dgn-gda:DGN5d1ce07ff708ea25c20a26e7a1a1b1f6 sio:SIO_000628 miriam-gene:4397 , lld:C0272236 ;
    a sio:SIO_001121 .
}
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_provenance {
  dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_assertion dcterms:description "[In this review we present data on clinical diseases with characteristic IgM abnormalities, including primary and secondary hyper IgM syndromes, autoimmune hemolytic anemia, cryoglobulinemia, primary biliary cirrhosis and multiple sclerosis and place the data in the perspective of the normal maturation of the immune response, including somatic mutation and genetic rearrangement.]. 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:22178509 ;
    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:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:52+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> ;
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}