@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0> .
@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:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_head {
  this: np:hasAssertion dgn-np:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_assertion;
    np:hasProvenance dgn-np:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_provenance;
    np:hasPublicationInfo dgn-np:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_assertion a np:Assertion .
  
  dgn-np:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_provenance a np:Provenance .
  
  dgn-np:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_assertion {
  miriam-gene:1400 a ncit:C16612 .
  
  lld:C0595905 a ncit:C7057 .
  
  dgn-gda:DGN42598796465ac0028a50908c2968377b sio:SIO_000628 miriam-gene:1400, lld:C0595905;
    a sio:SIO_001121 .
}

dgn-np:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_provenance {
  dgn-np:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_assertion dcterms:description
      "[The increase in Drp1, Fis1 and CypD and the decrease in Mfn1 and Mfn2 may be responsible for abnormal mitochondrial dynamics that we found in the cortex of HD patients, and may contribute to neuronal damage in HD patients.]. 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:21257639;
    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:NP471442.RAgJjcZklQBtdfFfm2Goz39AbjjCitkxoUjO2GPcv9FT0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:42+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" .
}