@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM> .
@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:NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM130_head {
  this: np:hasAssertion dgn-np:NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM130_assertion ;
    np:hasProvenance dgn-np:NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM130_provenance ;
    np:hasPublicationInfo dgn-np:NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM130_assertion a np:Assertion .
  dgn-np:NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM130_provenance a np:Provenance .
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}
dgn-np:NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM130_assertion {
  miriam-gene:3765 a ncit:C16612 .
  lld:C0011847 a ncit:C7057 .
  dgn-gda:DGNc8dfa252bc52d184dbca614c7823b6b8 sio:SIO_000628 miriam-gene:3765 , lld:C0011847 ;
    a sio:SIO_001121 .
}
dgn-np:NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM130_provenance {
  dgn-np:NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM130_assertion dcterms:description "[To assess the potential contribution of genetic alterations within KCNJ9 to diabetes susceptibility in the Pimas, we have genotyped 11 single nucleotide polymorphisms (SNPs) in 50 Pimas with diabetes and 50 Pimas over the age of 45 without diabetes and in 51 sib pairs, discordant for the disease, who were characterized by decreased allele sharing at the chromosomal location of the maximum LOD score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP543403.RABrOurjCCCjh2lu6yP99wcoQYZ-ZMaLmOw0Dw8eZxOaM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:28+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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> ;
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