@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U> .
@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:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_head {
  this: np:hasAssertion dgn-np:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_assertion;
    np:hasProvenance dgn-np:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_provenance;
    np:hasPublicationInfo dgn-np:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_assertion a np:Assertion .
  
  dgn-np:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_provenance a np:Provenance .
  
  dgn-np:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_assertion {
  miriam-gene:2950 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN9d8f565d0487d5393566923cd76926bd sio:SIO_000628 miriam-gene:2950, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_provenance {
  dgn-np:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_assertion dcterms:description
      "[Our work concludes that GSTM1, GSTT1 and GSTP1 variants might contribute to the development of T2DM and GSTT1 variant alone is involved in the development of T2DM associated CAD complications in the South Indian population.]. 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:21352813;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP761371.RAYJfuCLTGJbt2rf2nNz80J4fdd22Tx54VTHDPb8vx7_U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:41+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" .
}