@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_head {
  this: np:hasAssertion dgn-np:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_assertion ;
    np:hasProvenance dgn-np:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_provenance ;
    np:hasPublicationInfo dgn-np:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_assertion a np:Assertion .
  dgn-np:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_provenance a np:Provenance .
  dgn-np:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  lld:C1833104 a ncit:C7057 .
  dgn-gda:DGN03f2e7f087d6c730f55fd29e6568fb26 sio:SIO_000628 miriam-gene:3630 , lld:C1833104 ;
    a sio:SIO_001121 .
}
dgn-np:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_provenance {
  dgn-np:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_assertion dcterms:description "[Recent reports in the literature, all in the past year, have identified activating mutations in the KATP channel that prevent its closure and hence insulin secretion as the major cause of permanent neonatal diabetes mellitus.]. 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:16012265 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP503698.RAZNcwmI76dQ4_4OsPHheuUGJr8nGzZs7cXFTGqQzwwLc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:33+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}