@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM> .
@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 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:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_head {
  this: np:hasAssertion dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_assertion;
    np:hasProvenance dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_provenance;
    np:hasPublicationInfo dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_assertion a np:Assertion .
  
  dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_provenance a np:Provenance .
  
  dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_assertion {
  miriam-gene:8909 a ncit:C16612 .
  
  lld:C0018852 a ncit:C7057 .
  
  dgn-gda:DGNe5e877d87fb4c6e10c67d50b2b4fd6fa sio:SIO_000628 miriam-gene:8909, lld:C0018852;
    a sio:SIO_001121 .
}

dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_provenance {
  dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_assertion dct: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:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_publicationInfo {
  this: dct:created "2014-10-02T12:35:33+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}