@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg> .
@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:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_head {
  this: np:hasAssertion dgn-np:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion;
    np:hasProvenance dgn-np:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_provenance;
    np:hasPublicationInfo dgn-np:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion a np:Assertion .
  
  dgn-np:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_provenance a np:Provenance .
  
  dgn-np:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  
  lld:C0581883 a ncit:C7057 .
  
  dgn-gda:DGN622708458c546c4bb521bc5514455aa7 sio:SIO_000628 miriam-gene:3630, lld:C0581883;
    a sio:SIO_001121 .
}

dgn-np:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_provenance {
  dgn-np:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_assertion dcterms:description
      "[Monogenic forms of T2DM with profound defect in insulin secretion include subtypes of maturity onset diabetes of the young (MODY), maternally inherited diabetes with deafness (MIDD) caused by mitochondrial mutations, and rare cases resulting from insulin gene mutations.]. 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:15955369;
    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:NP594843.RAjPZefrfXFzfzSB0I8mHC4VlW4SVinMO_C3ntjH7OrIg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:57+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" .
}