@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk> .
@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:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_head {
  this: np:hasAssertion dgn-np:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_assertion;
    np:hasProvenance dgn-np:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_provenance;
    np:hasPublicationInfo dgn-np:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_assertion a np:Assertion .
  
  dgn-np:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_provenance a np:Provenance .
  
  dgn-np:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_assertion {
  miriam-gene:8091 a ncit:C16612 .
  
  lld:C1849524 a ncit:C7057 .
  
  dgn-gda:DGN74ec5f0b27d855101735ecbc8c44a462 sio:SIO_000628 miriam-gene:8091, lld:C1849524;
    a sio:SIO_001121 .
}

dgn-np:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_provenance {
  dgn-np:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_assertion dcterms:description
      "[Their pattern of expression in embryonal and adult tissues, the analysis of the `pygmy` phenotype induced by the inactivation of the HMGI-C gene, and their frequent qualitative or quantitative alteration in experimental and human tumors indicate their pivotal role in the control of cell growth, differentiation, and tumorigenesis in several tissues representative of the epithelial, mesenchymal, and hematopoietic lineages.]. 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:10344762;
    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:NP905544.RAtZ1YcklML_HKNbXZHFBXBsZnod8Gc64MtFCKGCvXdMk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:16+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" .
}