@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0> .
@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:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_head {
  this: np:hasAssertion dgn-np:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_assertion;
    np:hasProvenance dgn-np:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_provenance;
    np:hasPublicationInfo dgn-np:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_assertion a np:Assertion .
  
  dgn-np:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_provenance a np:Provenance .
  
  dgn-np:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_assertion {
  miriam-gene:7466 a ncit:C16612 .
  
  lld:C0524851 a ncit:C7057 .
  
  dgn-gda:DGN53efa5399322cb172d450746db1603e2 sio:SIO_000628 miriam-gene:7466, lld:C0524851;
    a sio:SIO_001121 .
}

dgn-np:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_provenance {
  dgn-np:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_assertion dcterms:description
      "[Mutations in WFS1 also cause Wolfram syndrome (WS), an autosomal recessive neurodegenerative disorder defined by diabetes mellitus, optic atrophy and often deafness, while numerous single nucleotide polymorphisms (SNPs) in WFS1 have been associated with increased risk for diabetes mellitus, psychiatric illnesses and Parkinson 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:18688868;
    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:NP776957.RAtb8fG8uPGA_yN3zZ7NfptuAREjVMg2pWCPkoL-5K9b0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:29+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" .
}