@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk> .
@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:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_head {
   this: np:hasAssertion dgn-np:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_assertion ;
    np:hasProvenance dgn-np:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_provenance ;
    np:hasPublicationInfo dgn-np:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_assertion a np:Assertion .
  dgn-np:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_provenance a np:Provenance .
  dgn-np:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_assertion {
   miriam-gene:6520 a ncit:C16612 .
  lld:C1531608 a ncit:C7057 .
  dgn-gda:DGN96182f0fa9efea4d49b715b872f6878f sio:SIO_000628 miriam-gene:6520 , lld:C1531608 ;
    a sio:SIO_001121 .
}
dgn-np:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_provenance {
   dgn-np:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_assertion dcterms:description "[Chromosomal translocations involving the immunoglobulin heavy chain gene (IgH) and nonrandom protooncogene loci are the hallmark of genetic alterations found not only in multiple myeloma (MM), but also in premalignant stages of MM, including monoclonal gammopathy of undetermined significance (MGUS) and smoldering myeloma (SMM).]. 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:12824903 ;
    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:NP416916.RASKqFmoFtHfpzz7t7YWoM68hFCVQ09iY_GSwAIEC7gCk130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:07+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" .
}