@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8> .
@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:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_head {
  this: np:hasAssertion dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_assertion ;
    np:hasProvenance dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_provenance ;
    np:hasPublicationInfo dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_assertion a np:Assertion .
  dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_provenance a np:Provenance .
  dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_assertion {
  miriam-gene:2328 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGN685ce21ae2b45696e8dab1ec63c939be sio:SIO_000628 miriam-gene:2328 , lld:C0020538 ;
    a sio:SIO_001122 .
}
dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_provenance {
  dgn-np:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_assertion dct:description "[tatistically significant heterogeneity in the relative frequencies of single and multiple site alleles, haplotypes, and genotypes of the human FMO3 among ethnic subdivisions suggests that population differences in the susceptibility of humans to abnormal metabolism or adverse drug reactions for chemicals metabolized by human FMO3 could exist.]. 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:11717182 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct: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" .
}