@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws> .
@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/v4.0.0/void/> .

dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_head {
  this: np:hasAssertion dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_assertion;
    np:hasProvenance dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_provenance;
    np:hasPublicationInfo dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_assertion a np:Assertion .
  
  dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_provenance a np:Provenance .
  
  dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_assertion {
  miriam-gene:6834 a ncit:C16612 .
  
  lld:C0268237 a ncit:C7057 .
  
  dgn-gda:DGN930acab1af6017090fe63aa95c674b79 sio:SIO_000628 miriam-gene:6834, lld:C0268237;
    a sio:SIO_001121 .
}

dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_provenance {
  dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_assertion dcterms:description
      "[These data confirm that the spectrum of MRI findings in LS is variable and that SURF1 mutations should be considered in patients with encephalomyopathy and COX deficiency even when early MRI findings are negative.]. 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:15214016;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:08+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}