@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E> .
@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:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_head {
  this: np:hasAssertion dgn-np:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_assertion;
    np:hasProvenance dgn-np:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_provenance;
    np:hasPublicationInfo dgn-np:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_assertion a np:Assertion .
  
  dgn-np:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_provenance a np:Provenance .
  
  dgn-np:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  
  lld:C0011849 a ncit:C7057 .
  
  dgn-gda:DGNa61177299dae03fe9fe41edd9f1c6a3c sio:SIO_000628 miriam-gene:3630, lld:C0011849;
    a sio:SIO_001121 .
}

dgn-np:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_provenance {
  dgn-np:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_assertion dcterms:description
      "[This mutation seemed to be maternally transmitted in the family, and the onset of diabetes was occurring earlier and the insulin secretory capacity was declining from generation to generation, so that these findings suggest that the point mutation at np 3316 is associated with various phenotypes of 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:10395242;
    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:NP256721.RArLxn0f-WDl6gLeMHzOHi2FjHyxJN9pgM5ER3te9ZF8E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:42+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" .
}