@prefix dc: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE> .
@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 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:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_head {
  this: np:hasAssertion dgn-np:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_assertion ;
    np:hasProvenance dgn-np:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_provenance ;
    np:hasPublicationInfo dgn-np:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_assertion a np:Assertion .
  dgn-np:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_provenance a np:Provenance .
  dgn-np:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_assertion {
  miriam-gene:51151 a ncit:C16612 .
  lld:C1704437 a ncit:C7057 .
  dgn-gda:DGNda13ee306106fe9a5f7399818f90f232 sio:SIO_000628 miriam-gene:51151 , lld:C1704437 ;
    a sio:SIO_001121 .
}
dgn-np:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_provenance {
  dgn-np:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_assertion dc:description "[In infants protected from RDS (those that had no RDS, despite extreme prematurity and lack of glucocorticoid therapy), compared with infants that had RDS develop despite having received glucocorticoid therapy, the frequencies of 6A2 (.22 vs.71), 6A3 (.72 vs.17), 6A2/1A0 (.17 vs.68), 6A3/1A1 (.39 vs.10), and 6A3/1A2 (.28 vs.06) in the two groups, respectively, were strikingly different.]. 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:10762543 ;
    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:NP808381.RAEV0e30OWRsv4s4_wNUfuZIr1HJ6DRUXvmaS4wYoYRmE130_publicationInfo {
  this: dc:created "2014-10-02T12:40:15+02:00"^^xsd:dateTime ;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dc:rightsHolder dgn-void:IBIGroup ;
    dc:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}