@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4> .
@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:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_head {
  this: np:hasAssertion dgn-np:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_assertion ;
    np:hasProvenance dgn-np:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_provenance ;
    np:hasPublicationInfo dgn-np:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_assertion a np:Assertion .
  dgn-np:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_provenance a np:Provenance .
  dgn-np:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_assertion {
  miriam-gene:5251 a ncit:C16612 .
  lld:C0282528 a ncit:C7057 .
  dgn-gda:DGNfb9a1eab8b70dd7dede6528b223ced7e sio:SIO_000628 miriam-gene:5251 , lld:C0282528 ;
    a sio:SIO_001121 .
}
dgn-np:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_provenance {
  dgn-np:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_assertion dcterms:description "[These studies have revealed important new insights regarding the mechanism of protein translocation across the peroxisomal membrane, the conservation of PEX genes through evolution, the role of peroxins in fatal human peroxisomal disorders, and the biogenesis of the organelle.]. 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:9457172 ;
    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:NP837904.RAYGHNsa9sokAV3OgITZcuaZZ-wGdCmXp19QXsZBsrSA4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:32+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" .
}