@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc> .
@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:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_head {
  this: np:hasAssertion dgn-np:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_assertion;
    np:hasProvenance dgn-np:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_provenance;
    np:hasPublicationInfo dgn-np:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_assertion a np:Assertion .
  
  dgn-np:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_provenance a np:Provenance .
  
  dgn-np:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_assertion {
  miriam-gene:833 a ncit:C16612 .
  
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    a sio:SIO_001121 .
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dgn-np:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_provenance {
  dgn-np:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_assertion dcterms:description
      "[Thus, associations identified in the GoKinD collections on chromosomes 11p15.4 (near the CARS gene) and 13q33.3 (within an intergenic region between MYO16 and IRS2) are susceptibility loci of kidney disease common to both type 1 and 2 diabetes.]. 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:21412220;
    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:NP244974.RARbzAR8maND182fZtnCARqV0Uw8dIt_JQnmd597zfOVc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:17+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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