@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg> .
@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/v3.0.0/void/> .

dgn-np:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_head {
  this: np:hasAssertion dgn-np:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_assertion;
    np:hasProvenance dgn-np:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_provenance;
    np:hasPublicationInfo dgn-np:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_assertion a np:Assertion .
  
  dgn-np:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_provenance a np:Provenance .
  
  dgn-np:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_assertion {
  miriam-gene:256471 a ncit:C16612 .
  
  lld:C0027877 a ncit:C7057 .
  
  dgn-gda:DGNd0a454310b88ad5ffc1271b5940882c2 sio:SIO_000628 miriam-gene:256471, lld:C0027877;
    a sio:SIO_001122 .
}

dgn-np:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_provenance {
  dgn-np:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_assertion dcterms:description
      "[The late-infantile-onset forms of neuronal ceroid lipofuscinosis (LINCL) are the most genetically heterogeneous group among the autosomal recessive neuronal ceroid lipofuscinoses (NCLs), with causative mutations found in CLN1, CLN2, CLN5, CLN6, CLN7 (MFSD8), and CLN8 genes.]. 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:19431184;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP981986.RACD3C7p2Qo7vaOvu7UIsn838aEoGmagJY69UcutF0GMg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:40+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}