@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU> .
@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:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_head {
  this: np:hasAssertion dgn-np:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_assertion;
    np:hasProvenance dgn-np:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_provenance;
    np:hasPublicationInfo dgn-np:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_assertion a np:Assertion .
  
  dgn-np:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_provenance a np:Provenance .
  
  dgn-np:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_assertion {
  miriam-gene:6833 a ncit:C16612 .
  
  lld:C0158981 a ncit:C7057 .
  
  dgn-gda:DGN20124f088bc33b4a207a92a169cdf2d5 sio:SIO_000628 miriam-gene:6833, lld:C0158981;
    a sio:SIO_001121 .
}

dgn-np:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_provenance {
  dgn-np:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_assertion dcterms:description
      "[Finally, the example of single gene diabetes, particularly HNF1A MODY and permanent neonatal diabetes associated with the KCNJ11 and ABCC8 genes, all efficiently controlled on sulfonylurea, inspires us to continue the efforts to tailor individual treatment for T2DM patients.]. 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:22996131;
    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:NP1014664.RAJnMECxWTTc_yiTucviqlTMDKm0RLQN9r4my63DH7LsU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:25+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" .
}