@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I> .
@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:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_head {
  this: np:hasAssertion dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_assertion ;
    np:hasProvenance dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_provenance ;
    np:hasPublicationInfo dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_assertion a np:Assertion .
  dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_provenance a np:Provenance .
  dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_assertion {
  miriam-gene:3767 a ncit:C16612 .
  lld:C0011849 a ncit:C7057 .
  dgn-gda:DGNce07e38bb40443fcb645827118b8d09d sio:SIO_000628 miriam-gene:3767 , lld:C0011849 ;
    a sio:SIO_001121 .
}
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_provenance {
  dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_assertion dcterms:description "[These results broaden the spectrum of diabetes phenotypes caused by mutations of KCNJ11 and suggest that mutations in this gene should be taken into consideration for not only permanent neonatal diabetes but also other forms of diabetes with milder phenotypes and later onset.]. 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:15784703 ;
    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:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:10+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" .
}