@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0> .
@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 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:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_head {
  this: np:hasAssertion dgn-np:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_assertion;
    np:hasProvenance dgn-np:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_provenance;
    np:hasPublicationInfo dgn-np:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_assertion a np:Assertion .
  
  dgn-np:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_provenance a np:Provenance .
  
  dgn-np:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_assertion {
  miriam-gene:1890 a ncit:C16612 .
  
  lld:C0241885 a ncit:C7057 .
  
  dgn-gda:DGN2cf9b66e7f7495e67b8bf7268c9895cd sio:SIO_000628 miriam-gene:1890, lld:C0241885;
    a sio:SIO_001121 .
}

dgn-np:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_provenance {
  dgn-np:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_assertion dcterms:description
      "[This study stresses the insidious heterogeneous clinical onset of some cases of MNGIE, expands the spectrum of the phenotype, and suggests considering MNGIE in the differential diagnosis of enteropathic arthritis, isolated exercise intolerance, and inflammatory polyneuropathies not responsive to the usual treatment.]. 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:21503690;
    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:NP933058.RANLjKFk9MF6v3jNHyzY6Fui1grZgQ89qD4CQrSJOLsN0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:32+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" .
}