@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY> .
@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:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_head {
  this: np:hasAssertion dgn-np:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_assertion;
    np:hasProvenance dgn-np:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_provenance;
    np:hasPublicationInfo dgn-np:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_assertion a np:Assertion .
  
  dgn-np:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_provenance a np:Provenance .
  
  dgn-np:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_assertion {
  miriam-gene:9927 a ncit:C16612 .
  
  lld:C0270921 a ncit:C7057 .
  
  dgn-gda:DGN6d5ff292dae0658755207b969ea58a3e sio:SIO_000628 miriam-gene:9927, lld:C0270921;
    a sio:SIO_001121 .
}

dgn-np:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_provenance {
  dgn-np:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_assertion dcterms:description
      "[This study also demonstrates the value of MFN2 studies in cases of congenital axonal neuropathy, especially in cases of dominant inheritance, severe clinical symptoms or additional symptoms such as optic atrophy.]. 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:19889647;
    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:NP773850.RAazgnW1aykDuhCuMX7XcrXuf8QWTVrUc78tEkahqaprY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:35+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" .
}