@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q> .
@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:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_head {
  this: np:hasAssertion dgn-np:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_assertion ;
    np:hasProvenance dgn-np:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_provenance ;
    np:hasPublicationInfo dgn-np:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_assertion a np:Assertion .
  dgn-np:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_provenance a np:Provenance .
  dgn-np:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_assertion {
  miriam-gene:114609 a ncit:C16612 .
  lld:C0018852 a ncit:C7057 .
  dgn-gda:DGN3a75f4a86035cdd1a416278e0c3cb70e sio:SIO_000628 miriam-gene:114609 , lld:C0018852 ;
    a sio:SIO_001121 .
}
dgn-np:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_provenance {
  dgn-np:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_assertion dcterms:description "[Alpha heavy chain diseases (HCD) are lymphoproliferative disorders characterized by the production of truncated alpha immunoglobulin heavy chain without associated light chains, alpha HCD MAL is featured by multiple structural alterations of the alpha 1 productive gene and on original t(9;14)(p11;q32) translocation involving the other rearranged alpha 1 allele.]. 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:2125275 ;
    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:NP688579.RAxIJAzsY8Q8cDIyFpbtqGSvdxljbMyOopZ9bWiQ_AP2Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:58+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" .
}