@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU> .
@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:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_head {
  this: np:hasAssertion dgn-np:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_assertion;
    np:hasProvenance dgn-np:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_provenance;
    np:hasPublicationInfo dgn-np:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_assertion a np:Assertion .
  
  dgn-np:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_provenance a np:Provenance .
  
  dgn-np:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGN6181e7e6a82dfa5444847fdb596bb7b2 sio:SIO_000628 miriam-gene:1636, lld:C0038454;
    a sio:SIO_001122 .
}

dgn-np:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_provenance {
  dgn-np:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_assertion dcterms:description
      "[ It is suggested that ACE gene I/D polymorphism is a susceptible gene for stroke in DM2 patients in China. AT1R gene A1166C polymorphism contributes to the development of stroke in DM2 patients, but it is not an independent risk factor. There is synergistic effect of AT1R A1166C and ACE I/D gene polymorphisms on the occurrence and development of stroke in type 2 diabetics in China.]. 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:11774217;
    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:NP49436.RAiSSWEVKHPCz0vUWFiTXTFYtORC-mW3q5UkUohFxdGAU130_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" .
}