@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY> .
@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/v3.0.0/void/> .
dgn-np:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_head {
  this: np:hasAssertion dgn-np:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_assertion ;
    np:hasProvenance dgn-np:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_provenance ;
    np:hasPublicationInfo dgn-np:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_assertion a np:Assertion .
  dgn-np:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_provenance a np:Provenance .
  dgn-np:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_assertion {
  miriam-gene:346171 a ncit:C16612 .
  lld:C0011847 a ncit:C7057 .
  dgn-gda:DGN487b524873c0d595e72af450b1b8575d sio:SIO_000628 miriam-gene:346171 , lld:C0011847 ;
    a sio:SIO_001121 .
}
dgn-np:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_provenance {
  dgn-np:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_assertion dcterms:description "[The variable clinical features of TNDM1 may be associated with variation in the nature of the underlying epigenetic and genetic mutations, and future study of this disorder is likely to yield further insights not only into the biological mechanisms of imprinting, but also into the contribution of epigenetics to 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:20803656 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP986641.RAtq7a9_ydG3jnnAFEqztrTDaPVYtjovvBcvrIejmMiAY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:44+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}