@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90> .
@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:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_head {
  this: np:hasAssertion dgn-np:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_assertion ;
    np:hasProvenance dgn-np:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_provenance ;
    np:hasPublicationInfo dgn-np:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_assertion a np:Assertion .
  dgn-np:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_provenance a np:Provenance .
  dgn-np:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_assertion {
  miriam-gene:8163 a ncit:C16612 .
  lld:C0024790 a ncit:C7057 .
  dgn-gda:DGN27b31757d55ac16094139ee0c8fd6c14 sio:SIO_000628 miriam-gene:8163 , lld:C0024790 ;
    a sio:SIO_001121 .
}
dgn-np:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_provenance {
  dgn-np:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_assertion dcterms:description "[To test the applicability of clonotypic assays, we developed rational molecular methods for the detection of immunodominant clonotypes in blood and in historic marrow biopsies of 35 AA, 37 MDS, and 21 paroxysmal nocturnal hemoglobinuria (PNH) patients, in whom specific CDR3 sequences and clonal sizes were determined.]. 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:16614248 ;
    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:NP628488.RAj-pkD2y1QwOp8yS-pnPXSHd1HYsIwDc8PxtImO9Bx90130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:19+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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}