@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s> .
@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:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_head {
  this: np:hasAssertion dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_assertion;
    np:hasProvenance dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_provenance;
    np:hasPublicationInfo dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_assertion a np:Assertion .
  
  dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_provenance a np:Provenance .
  
  dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_assertion {
  miriam-gene:10934 a ncit:C16612 .
  
  lld:C0272236 a ncit:C7057 .
  
  dgn-gda:DGN0131000e1d6158d3ec30c2e76467c1f7 sio:SIO_000628 miriam-gene:10934, lld:C0272236;
    a sio:SIO_001121 .
}

dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_provenance {
  dgn-np:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_assertion dcterms:description
      "[The delineation of hyper-IgM syndromes made it possible to better define the mechanisms underlying the two major events of antibody maturation in humans, CSR and introduction of somatic hypermutation (SHM) in the variable region of immunoglobulins.]. 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:15661022;
    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:NP761040.RA4RC25ChstOX2mcfdl0nhDb-wcAuoXkbEKCSCUAArq7s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:40+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" .
}