@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc> .
@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:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_head {
  this: np:hasAssertion dgn-np:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_assertion;
    np:hasProvenance dgn-np:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_provenance;
    np:hasPublicationInfo dgn-np:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_assertion a np:Assertion .
  
  dgn-np:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_provenance a np:Provenance .
  
  dgn-np:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_assertion {
  miriam-gene:1476 a ncit:C16612 .
  
  lld:C0036572 a ncit:C7057 .
  
  dgn-gda:DGNa7d11a878296b41c86f18fb59f93813a sio:SIO_000628 miriam-gene:1476, lld:C0036572;
    a sio:SIO_001121 .
}

dgn-np:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_provenance {
  dgn-np:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_assertion dcterms:description
      "[Because cystatin B inhibits a class of lysosomal cysteine proteases called cathepsins, we hypothesized that increased proteolysis by one or more of these cathepsins is likely to be responsible for the seizure, ataxia, and neuronal apoptosis phenotypes characteristic of EPM1.]. 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:12918016;
    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:NP604602.RAGPJvCcY7sGy8KKkMzhlM8FSrMHZXHh-n6NpvvWsMnvc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:03+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" .
}