@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0> .
@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:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_head {
  this: np:hasAssertion dgn-np:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_assertion;
    np:hasProvenance dgn-np:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_provenance;
    np:hasPublicationInfo dgn-np:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_assertion a np:Assertion .
  
  dgn-np:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_provenance a np:Provenance .
  
  dgn-np:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0268596 a ncit:C7057 .
  
  dgn-gda:DGNe42fe2a501b714a81dfea80d11369a5b sio:SIO_000628 miriam-gene:675, lld:C0268596;
    a sio:SIO_001121 .
}

dgn-np:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_provenance {
  dgn-np:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_assertion dcterms:description
      "[Our results provide a structural and functional framework that could help to elucidate the role that an increased cellular FAD content obtained from riboflavin supplementation may play in the molecular pathogenesis of not only MADD, but genetic disorders of flavoproteins in general.]. 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:19088074;
    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:NP196865.RAYAxVI1V62kUAFOuwlY30Dnw-a66NhpXDKif6jN8kRr0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:48+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" .
}