@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA> .
@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:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_head {
  this: np:hasAssertion dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_assertion ;
    np:hasProvenance dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_provenance ;
    np:hasPublicationInfo dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_assertion a np:Assertion .
  dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_provenance a np:Provenance .
  dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_assertion {
  miriam-gene:6520 a ncit:C16612 .
  lld:C0019829 a ncit:C7057 .
  dgn-gda:DGN70b908789d90192a40f2bb1c08c3814a sio:SIO_000628 miriam-gene:6520 , lld:C0019829 ;
    a sio:SIO_001121 .
}
dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_provenance {
  dgn-np:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_assertion dcterms:description "[In an attempt to determine the clonality of L & H cells and to clarify the link between NLPHD and complicating LCL, we used polymerase chain reaction (PCR) to analyze 33 cases of NLPHD, including 15 cases with simultaneous or subsequent LCL, for clonal immunoglobulin (lg) heavy chain variable region (VH) gene rearrangements.]. 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:8630407 ;
    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:NP232636.RAGp3WCPe0Zy3ZbNSvA8_EyRf7hTWWD35hyOlFJLC-fwA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+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" .
}