@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M> .
@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:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_head {
  this: np:hasAssertion dgn-np:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_assertion;
    np:hasProvenance dgn-np:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_provenance;
    np:hasPublicationInfo dgn-np:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_assertion a np:Assertion .
  
  dgn-np:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_provenance a np:Provenance .
  
  dgn-np:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_assertion {
  miriam-gene:6712 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGNcaae6584bf6a9f4f16b27b92ffd74441 sio:SIO_000628 miriam-gene:6712, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_provenance {
  dgn-np:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_assertion dcterms:description
      "[We also examined a mouse knockout of β-III spectrin in which ataxia and progressive degeneration of cerebellar Purkinje cells has been previously reported and found morphological abnormalities in neurons from prefrontal cortex and deficits in object recognition tasks, consistent with the human cognitive phenotype.]. 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:23236289;
    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:NP281310.RAOAs0AeDDSuQ8zJQpSBKpbHJg308K4Zu2NDr5eXRgZ7M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:38+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" .
}