@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc> .
@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:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_head {
  this: np:hasAssertion dgn-np:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_assertion;
    np:hasProvenance dgn-np:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_provenance;
    np:hasPublicationInfo dgn-np:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_assertion a np:Assertion .
  
  dgn-np:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_provenance a np:Provenance .
  
  dgn-np:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_assertion {
  miriam-gene:6833 a ncit:C16612 .
  
  lld:C0085207 a ncit:C7057 .
  
  dgn-gda:DGN415ec69ed197dc34072fdd2ed696cebb sio:SIO_000628 miriam-gene:6833, lld:C0085207;
    a sio:SIO_001122 .
}

dgn-np:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_provenance {
  dgn-np:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_assertion dcterms:description
      "[It suggests that the defect in SUR1 gene (cc and AA) may contribute to insulin hypersecretion, which might be the cause of increased body weight and decreased insulin sensitivity and genotype cc of SUR1 is connected with severe type of GDM.]. 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:15840308;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP49757.RA6iH_n8y0reJ1iS-ifB-uFd9E80MrF0tSfYHC5H9wpPc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}