@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA> .
@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:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_head {
  this: np:hasAssertion dgn-np:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_assertion ;
    np:hasProvenance dgn-np:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_provenance ;
    np:hasPublicationInfo dgn-np:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_assertion a np:Assertion .
  dgn-np:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_provenance a np:Provenance .
  dgn-np:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_assertion {
  miriam-gene:3159 a ncit:C16612 .
  lld:C0086692 a ncit:C7057 .
  dgn-gda:DGN8816761e4f4ac26fc66733065e712938 sio:SIO_000628 miriam-gene:3159 , lld:C0086692 ;
    a sio:SIO_001121 .
}
dgn-np:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_provenance {
  dgn-np:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_assertion dcterms:description "[Because genes of the high-mobility group protein family HMGI(Y) are known to be involved in the development of a variety of benign solid tumors, it was the aim of the present study to analyze breakpoints of clonal chromosome abnormalities in that group of benign tumors for a possible correlation with retropseudogenes of the HMGIY gene.]. 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:11672774 ;
    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:NP822218.RAzQaa2JP9lwDdwhLUsoAl1icacn-ZP8v2jaFttm3NAkA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:23+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: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" .
}