@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE> .
@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/v3.0.0/void/> .

dgn-np:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_head {
  this: np:hasAssertion dgn-np:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_assertion;
    np:hasProvenance dgn-np:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_provenance;
    np:hasPublicationInfo dgn-np:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_assertion a np:Assertion .
  
  dgn-np:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_provenance a np:Provenance .
  
  dgn-np:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_assertion {
  miriam-gene:3659 a ncit:C16612 .
  
  lld:C3489413 a ncit:C7057 .
  
  dgn-gda:DGNb6e7c308c2687e9b5d9bb5866578efc9 sio:SIO_000628 miriam-gene:3659, lld:C3489413;
    a sio:SIO_001121 .
}

dgn-np:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_provenance {
  dgn-np:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_assertion dcterms:description
      "[Using a chromosome walking approach combined with fluorescence in situ hybridization analysis, we were able to show that the chromosome 12 breakpoints involved in uterine leiomyoma, pleomorphic adenoma of the salivary gland, and lipoma cluster to the same chromosomal region, which we therefore designated MAR (multiple-aberration region).]. 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:8527387;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP514584.RAKIjYMzztM4qCYsNOU4sZ2WXr8Mf4VvDNbMCVaWZwrvE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:44+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}