@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E> .
@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/v3.0.0/void/> .

dgn-np:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_head {
  this: np:hasAssertion dgn-np:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_assertion;
    np:hasProvenance dgn-np:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_provenance;
    np:hasPublicationInfo dgn-np:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_assertion a np:Assertion .
  
  dgn-np:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_provenance a np:Provenance .
  
  dgn-np:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0038644 a ncit:C7057 .
  
  dgn-gda:DGNe9e3ef1b681ff719a42968269b61c92b sio:SIO_000628 miriam-gene:2952, lld:C0038644;
    a sio:SIO_001122 .
}

dgn-np:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_provenance {
  dgn-np:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_assertion dcterms:description
      "[The frequencies of CYP2D6 mutant genotypes and the null genotypes for GSTM1 and GSTT1 were not different among SIDS victims compared to normal controls, and thus these polymorphisms are unlikely to identify families with a high risk of SIDS.]. 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:9069041;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP440562.RA-yvmULaq2vq3R-LK1mp2gSgTKw5nkOceevbanY1uf4E130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:57+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: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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}