@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0> .
@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:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_head {
  this: np:hasAssertion dgn-np:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_assertion;
    np:hasProvenance dgn-np:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_provenance;
    np:hasPublicationInfo dgn-np:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_assertion a np:Assertion .
  
  dgn-np:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_provenance a np:Provenance .
  
  dgn-np:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0011881 a ncit:C7057 .
  
  dgn-gda:DGNb301ec434739af206986881d782a3c00 sio:SIO_000628 miriam-gene:1636, lld:C0011881;
    a sio:SIO_001122 .
}

dgn-np:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_provenance {
  dgn-np:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_assertion dcterms:description
      "[SNPs Met235Thr in angiotensinogen, T>C (-344) in aldosterone synthase, and G>A (-1903) in chymase genes are significantly associated with diabetic chronic renal insufficiency in Indian patients and warrant replication in larger sample sets. Use of such markers for prediction of susceptibility to diabetes specific renal disease in the ethnically Indian popula]. 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:16672053;
    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:NP49394.RAooQxeka0Yih-K96AgvA-2DxoQbHwuUPMeauHRIR1LV0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}