@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY> .
@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:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_head {
  this: np:hasAssertion dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_assertion ;
    np:hasProvenance dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_provenance ;
    np:hasPublicationInfo dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_provenance a np:Provenance .
  dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_assertion {
  miriam-gene:157570 a ncit:C16612 .
  lld:C0392475 a ncit:C7057 .
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}
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_provenance {
  dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_assertion dcterms:description "[Since ESCO2 has been identified as the gene defective in the rare autosomal recessive cohesinopathy Roberts syndrome (RBS), cells from RBS patients can be used to elucidate the role of ESCO2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:25+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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