@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js> .
@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:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_head {
  this: np:hasAssertion dgn-np:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_assertion;
    np:hasProvenance dgn-np:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_provenance;
    np:hasPublicationInfo dgn-np:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_assertion a np:Assertion .
  
  dgn-np:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_provenance a np:Provenance .
  
  dgn-np:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_assertion {
  miriam-gene:617 a ncit:C16612 .
  
  lld:C0342778 a ncit:C7057 .
  
  dgn-gda:DGN105643fd213ce608ac1d5dff93dcab4b sio:SIO_000628 miriam-gene:617, lld:C0342778;
    a sio:SIO_001121 .
}

dgn-np:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_provenance {
  dgn-np:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_assertion dcterms:description
      "[Interestingly, the British and Turkish patients had complex III deficiency, whereas in the Finnish patients with GRACILE syndrome complex III activity was within the normal range, implying that BCS1L has another cellular function that is uncharacterized but essential and is putatively involved in iron metabolism.]. 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:12215968;
    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:NP691635.RAMJVDvV8sknC55cw4ShAdtjwDt6SCkOU4ElFHmVMT4js130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:00+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" .
}