@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY> .
@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:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_head {
  this: np:hasAssertion dgn-np:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_assertion;
    np:hasProvenance dgn-np:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_provenance;
    np:hasPublicationInfo dgn-np:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_assertion a np:Assertion .
  
  dgn-np:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_provenance a np:Provenance .
  
  dgn-np:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGN09a175ce7bace8a896ae38fa191af52b sio:SIO_000628 miriam-gene:3342, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_provenance {
  dgn-np:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_assertion dcterms:description
      "[We have analyzed the frequency and prognostic impact of genetic changes as detected by CGH and evaluated the relationship between these chromosomal imbalances and IGH translocation, analyzed by FISH, in 74 patients with newly diagnosed MM.]. 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:15238415;
    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:NP440720.RAAio43vxUeiFSRq5kX13xpT7Tv7QYBAvViBhhyWEcVfY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:20+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" .
}