@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE> .
@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:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_head {
  this: np:hasAssertion dgn-np:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_assertion;
    np:hasProvenance dgn-np:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_provenance;
    np:hasPublicationInfo dgn-np:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_assertion a np:Assertion .
  
  dgn-np:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_provenance a np:Provenance .
  
  dgn-np:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGN2c2acbf063df3b9baa7e038c9780b710 sio:SIO_000628 miriam-gene:3133, lld:C0011847;
    a sio:SIO_001121 .
}

dgn-np:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_provenance {
  dgn-np:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_assertion dcterms:description
      "[However, in both humans and mouse models of this disease, one of the principle determining genetic factors in diabetes incidence is the inheritance of mutant MHC class II alleles that are associated with increased occurrence of disease.]. 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:18679630;
    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:NP457610.RAS3iM8xAAl96tY6gucTGR5xWWMHKJAa4yt62jk1S-mEE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:08+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" .
}