@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc> .
@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:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_head {
  this: np:hasAssertion dgn-np:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_assertion;
    np:hasProvenance dgn-np:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_provenance;
    np:hasPublicationInfo dgn-np:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_assertion a np:Assertion .
  
  dgn-np:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_provenance a np:Provenance .
  
  dgn-np:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_assertion {
  miriam-gene:1559 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNc49475a3187ed88f2ff357f13225e4e9 sio:SIO_000628 miriam-gene:1559, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_provenance {
  dgn-np:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_assertion dcterms:description
      "[Allelic discrimination assays based on fluorescent PCR gave entire satisfaction for CYP2C9 and MDR1 genotyping. This reliable genotyping strategy can be easily used in clinical practice and should be further developed for additional SNPs identification.]. 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:12805007;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP54922.RAQ2Xgm_U9W_k4gpb0ADE91USTJeKPCDDM0vZxbC-0stc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:10+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" .
}