@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_head {
  this: np:hasAssertion dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_assertion;
    np:hasProvenance dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_provenance;
    np:hasPublicationInfo dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_assertion a np:Assertion .
  
  dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_provenance a np:Provenance .
  
  dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_assertion {
  miriam-gene:213 a ncit:C16612 .
  
  lld:C0391861 a ncit:C7057 .
  
  dgn-gda:DGNfdf6e84490426d366212a26ba76ec25d sio:SIO_000628 miriam-gene:213, lld:C0391861;
    a sio:SIO_001121 .
}

dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_provenance {
  dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_assertion dcterms:description
      "[The objective of this study was to investigate the mutational change in chromosome 13 (13q14) among Sudanese MM patients and to identify the association between extent of plasma cell infiltration in the bone marrow, albumin level and deletion of 13q14 by an analytical case control study.]. 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:26277665;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:32+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}