@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ> .
@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:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_head {
  this: np:hasAssertion dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_assertion;
    np:hasProvenance dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_provenance;
    np:hasPublicationInfo dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_assertion a np:Assertion .
  
  dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_provenance a np:Provenance .
  
  dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_assertion {
  miriam-gene:11132 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN72421873fda076688d24f6996d1694b8 sio:SIO_000628 miriam-gene:11132, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_provenance {
  dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_assertion dcterms:description
      "[The association of the polymorphisms Gly972Arg, SNP43, and Pro12Ala, of the genes IRS1, CAPN10, PPARG2, with the risk of failure to sulphonylurea and metformin therapies was determinated in patients with DT2 in Yucatn, Mxico.]. 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:19418728;
    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:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}