@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU> .
@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:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_head {
  this: np:hasAssertion dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_assertion;
    np:hasProvenance dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_provenance;
    np:hasPublicationInfo dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_assertion a np:Assertion .
  
  dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_provenance a np:Provenance .
  
  dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_assertion {
  miriam-gene:79612 a ncit:C16612 .
  
  lld:C0015230 a ncit:C7057 .
  
  dgn-gda:DGN3cf95e99799628da22b3fd030a81d5bc sio:SIO_000628 miriam-gene:79612, lld:C0015230;
    a sio:SIO_001121 .
}

dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_provenance {
  dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_assertion dcterms:description
      "[Despite careful medical record review and full resequencing of the NAT2 coding region, we found no association of NAT2 coding alleles with sulfonamide hypersensitivity (predominantly cutaneous eruptions) in this adult Caucasian population.]. 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:22850190;
    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:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:00+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" .
}