@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ> .
@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:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_head {
  this: np:hasAssertion dgn-np:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_assertion;
    np:hasProvenance dgn-np:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_provenance;
    np:hasPublicationInfo dgn-np:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_assertion a np:Assertion .
  
  dgn-np:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_provenance a np:Provenance .
  
  dgn-np:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_assertion {
  miriam-gene:1404 a ncit:C16612 .
  
  lld:C0002793 a ncit:C7057 .
  
  dgn-gda:DGN589501239f157b2edb7e67e6af9a5d0a sio:SIO_000628 miriam-gene:1404, lld:C0002793;
    a sio:SIO_001121 .
}

dgn-np:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_provenance {
  dgn-np:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_assertion dcterms:description
      "[Second, during dedifferentiation of HACs by passage in monolayer cell culture, during which the expression of SOX9 progressively decreased, four of the genes (S100A1, RGC32, CRTL1 and SPINT1) also decreased in their expression.]. 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:17935617;
    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:NP246695.RA0eSHCpFctD4XpR9so8xke2BnvW1A_Wouovyw1ifukzQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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" .
}