@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE> .
@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:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_head {
  this: np:hasAssertion dgn-np:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_assertion;
    np:hasProvenance dgn-np:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_provenance;
    np:hasPublicationInfo dgn-np:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_assertion a np:Assertion .
  
  dgn-np:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_provenance a np:Provenance .
  
  dgn-np:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_assertion {
  miriam-gene:3495 a ncit:C16612 .
  
  lld:C0023434 a ncit:C7057 .
  
  dgn-gda:DGN4392996aa38eb070b0a94a0594313f1e sio:SIO_000628 miriam-gene:3495, lld:C0023434;
    a sio:SIO_001121 .
}

dgn-np:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_provenance {
  dgn-np:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_assertion dcterms:description
      "[These results document that the IGHD and IGHJ gene biases in the CLL expressed VH CDR3 repertoire are not stochastic but are directed by selection operating at the immunoglobulin protein level.]. 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:21968789;
    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:NP310955.RAghXi839KzxfGM9YTQWbyiHMnq29k6JAKCafIYt_4fvE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:58+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" .
}