@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM> .
@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:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_head {
  this: np:hasAssertion dgn-np:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_assertion;
    np:hasProvenance dgn-np:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance;
    np:hasPublicationInfo dgn-np:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_assertion a np:Assertion .
  
  dgn-np:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance a np:Provenance .
  
  dgn-np:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_assertion {
  miriam-gene:155 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN34a318204947243c862fb74d083d578f sio:SIO_000628 miriam-gene:155, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance {
  dgn-np:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_assertion dcterms:description
      "[Variants located within the gene TCF7L2 are strongly associated with T2D but not with MS, providing support to previous evidence indicating that polymorphisms at the TCF7L2 gene increase T2D risk. In contrast, the non-synonymous ADRB3 rs4994 polymorphism is associated with T2D and MS.]. 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:20503258;
    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:NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_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" .
}