@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw> .
@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:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_head {
  this: np:hasAssertion dgn-np:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_assertion;
    np:hasProvenance dgn-np:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_provenance;
    np:hasPublicationInfo dgn-np:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_assertion a np:Assertion .
  
  dgn-np:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_provenance a np:Provenance .
  
  dgn-np:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_assertion {
  miriam-gene:8091 a ncit:C16612 .
  
  lld:C0042133 a ncit:C7057 .
  
  dgn-gda:DGNa4dfd6e58f5f58a433be9dbf8fc05d8a sio:SIO_000628 miriam-gene:8091, lld:C0042133;
    a sio:SIO_001121 .
}

dgn-np:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_provenance {
  dgn-np:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_assertion dcterms:description
      "[Fluorescence in situ hybridization revealed three copies of HMGIC (alias HMGA2), two on the normal chromosomes 12 at 12q15, as well as another on the der(14) in the breakpoint region, suggesting that the 12q breakpoint occurred 5' (centromeric) to HMGIC (HMGA2), as has been frequently observed in uterine leiomyoma.]. 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:11904348;
    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:NP348730.RAHdnS27ztWrU0oEKr2UJeMAFJ1xTGXsP3nTSqVi_OOtw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:23+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" .
}