@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo> .
@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:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_head {
  this: np:hasAssertion dgn-np:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_assertion;
    np:hasProvenance dgn-np:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_provenance;
    np:hasPublicationInfo dgn-np:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_assertion a np:Assertion .
  
  dgn-np:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_provenance a np:Provenance .
  
  dgn-np:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_assertion {
  miriam-gene:10 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN8bb9b67b1075938280c59e63c47af327 sio:SIO_000628 miriam-gene:10, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_provenance {
  dgn-np:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_assertion dcterms:description
      "[The distribution of NAT2 activity in the healthy control group was found to be correlated with that of healthy caucasians. Patients had slow acetylator phenotypes of NAT2, 1.8 times higher than controls but no statistical differences were found (p=0.07). In addition, the NAT2*5 alelle was more statistically correlated with breast cancer patients rather than the controls (p=0.02). Moreover, NAT2*5B was the most frequent haplotype of the NAT2*5 family (p=0.000). Breast cancer patients were detected to posses more CYP1B1*3 mutant alleles than the controls (p=0.043). The combined effect of CYP1B1*3 polymorphism and NAT2 slow acetylator genotype contributed to an increased risk for breast cancer in patients in this study (p=0.004).]. 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:20683028;
    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:NP54024.RAbelkiZh9Yu50XcBsZhToG2Ice6cDEaE0qkCV_NIyndo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}