@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o> .
@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 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:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_head {
  this: np:hasAssertion dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_assertion;
    np:hasProvenance dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_provenance;
    np:hasPublicationInfo dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_assertion a np:Assertion .
  
  dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_provenance a np:Provenance .
  
  dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGNc38a0f4f92637d0e836e999df2dc7aba sio:SIO_000628 miriam-gene:3630, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_provenance {
  dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_assertion dcterms:description
      "[Single nucleotide polymorphisms (SNPs) in the calpain-10 gene (CAPN-10), which encodes a protein involved in the secretion and action of insulin, and chronic exposure to inorganic arsenic (iAs) through drinking water have been independently associated with an increase in the risk for T2DM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:23349674;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:07+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 orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}