@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k> .
@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:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_head {
  this: np:hasAssertion dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_assertion;
    np:hasProvenance dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_provenance;
    np:hasPublicationInfo dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_assertion a np:Assertion .
  
  dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_provenance a np:Provenance .
  
  dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_assertion {
  miriam-gene:8091 a ncit:C16612 .
  
  lld:C1306242 a ncit:C7057 .
  
  dgn-gda:DGNcb45b54ce14ffae6a59173f504901b96 sio:SIO_000628 miriam-gene:8091, lld:C1306242;
    a sio:SIO_001121 .
}

dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_provenance {
  dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_assertion dcterms:description
      "[To shed more light on the pathobiology of aggressive angiomyxoma and to investigate the molecular mechanisms behind the involvement of the HMGA2 gene in this tumor type (fusion transcript vs deregulated expression), we investigated, cytogenetically and with molecular techniques, one such tumor which presented a t(11;12)(q23;q15) as the sole karyotypic aberration.]. 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:16568309;
    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:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:09+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" .
}