@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio> .
@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:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_head {
  this: np:hasAssertion dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_assertion;
    np:hasProvenance dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_provenance;
    np:hasPublicationInfo dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_assertion a np:Assertion .
  
  dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_provenance a np:Provenance .
  
  dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_assertion {
  miriam-gene:224 a ncit:C16612 .
  
  lld:C0037231 a ncit:C7057 .
  
  dgn-gda:DGNf59bf1b3648bdcf1e04ad41a4cdc3762 sio:SIO_000628 miriam-gene:224, lld:C0037231;
    a sio:SIO_001121 .
}

dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_provenance {
  dgn-np:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_assertion dcterms:description
      "[Sjögren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder caused by mutations in the ALDH3A2 gene that encodes fatty aldehyde dehydrogenase (FALDH), an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid.]. 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:16996289;
    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:NP234920.RAsi3izhx-h-vJntBzcfqrh4NvP5Pu6gejYqEYHfscDio130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:53+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" .
}