@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU> .
@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:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_head {
  this: np:hasAssertion dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_assertion;
    np:hasProvenance dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_provenance;
    np:hasPublicationInfo dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_assertion a np:Assertion .
  
  dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_provenance a np:Provenance .
  
  dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_assertion {
  miriam-gene:1201 a ncit:C16612 .
  
  lld:C0085078 a ncit:C7057 .
  
  dgn-gda:DGN5b89409239463d26a8075e97e329df9c sio:SIO_000628 miriam-gene:1201, lld:C0085078;
    a sio:SIO_001121 .
}

dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_provenance {
  dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_assertion dcterms:description
      "[To use the Unified Batten Disease Rating Scale (UBDRS) to measure the rate of decline in physical and functional capability domains in patients with juvenile neuronal ceroid lipofuscinosis (JNCL) or Batten disease, a neurodegenerative lysosomal storage disorder.]. 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:22013180;
    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:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:07+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" .
}