@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1235249.RAHLqHuKK8EEqEOg192rVDw-ru2CsPpFLzxFOaWGV6qaM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1235249.RAHLqHuKK8EEqEOg192rVDw-ru2CsPpFLzxFOaWGV6qaM130_head {
  this: np:hasAssertion dgn-np:NP1235249.RAHLqHuKK8EEqEOg192rVDw-ru2CsPpFLzxFOaWGV6qaM130_assertion;
    np:hasProvenance dgn-np:NP1235249.RAHLqHuKK8EEqEOg192rVDw-ru2CsPpFLzxFOaWGV6qaM130_provenance;
    np:hasPublicationInfo dgn-np:NP1235249.RAHLqHuKK8EEqEOg192rVDw-ru2CsPpFLzxFOaWGV6qaM130_publicationInfo;
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    a np:PublicationInfo .
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dgn-np:NP1235249.RAHLqHuKK8EEqEOg192rVDw-ru2CsPpFLzxFOaWGV6qaM130_assertion {
  miriam-gene:150165 a ncit:C16612 .
  
  lld:C1274282 a ncit:C7057 .
  
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dgn-np:NP1235249.RAHLqHuKK8EEqEOg192rVDw-ru2CsPpFLzxFOaWGV6qaM130_provenance {
  dgn-np:NP1235249.RAHLqHuKK8EEqEOg192rVDw-ru2CsPpFLzxFOaWGV6qaM130_assertion dcterms:description
      "[We validated three SNPs (rs78142040, rs9605146 and rs3848719) in additional ARDS patients to substantiate their associations with susceptibility, severity and outcome of ARDS. rs78142040 (C&gt;T) occurs within a histone mark (intron 6) of the Arylsulfatase D gene. rs9605146 (G&gt;A) causes a deleterious coding change (proline to leucine) in the XK, Kell blood group complex subunit-related family, member 3 gene. rs3848719 (G&gt;A) is a synonymous SNP in the Zinc-Finger/Leucine-Zipper Co-Transducer NIF1 gene. rs78142040, rs9605146, and rs3848719 are associated significantly with susceptibility to ARDS. rs3848719 is associated with APACHE II score quartile. rs78142040 is associated with 60-day mortality in the overall ARDS patient population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1235249.RAHLqHuKK8EEqEOg192rVDw-ru2CsPpFLzxFOaWGV6qaM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:06+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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    prv:usedData dgn-void:disgenetv3.0rdf;
    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>;
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    pav:version "v4.0.0.0" .
  
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}