@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk> .
@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:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_head {
  this: np:hasAssertion dgn-np:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_assertion;
    np:hasProvenance dgn-np:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_provenance;
    np:hasPublicationInfo dgn-np:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_assertion a np:Assertion .
  
  dgn-np:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_provenance a np:Provenance .
  
  dgn-np:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGN66eda5ab011a04dc1f9973b5aec79f5f sio:SIO_000628 miriam-gene:595, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_provenance {
  dgn-np:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_assertion dcterms:description
      "[Our results confirm previous findings that the 11q13 breakpoints in MM are scattered throughout the 11q13 region encompassing the cyclin D1 gene, thus suggesting the absence of 11q13 breakpoint clusters in 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:9949176;
    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:NP201665.RAVuOjkamRRi9_is9-WaxaqK7vol1eyrGs2AZANgPSzZk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:51+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" .
}