@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU> .
@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/v4.0.0/void/> .
dgn-np:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_head {
  this: np:hasAssertion dgn-np:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_assertion ;
    np:hasProvenance dgn-np:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_provenance ;
    np:hasPublicationInfo dgn-np:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_assertion a np:Assertion .
  dgn-np:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_provenance a np:Provenance .
  dgn-np:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_assertion {
  miriam-gene:540 a ncit:C16612 .
  lld:C0019202 a ncit:C7057 .
  dgn-gda:DGN260bf1d1f8c1cc661bbcabb1ba83aab1 sio:SIO_000628 miriam-gene:540 , lld:C0019202 ;
    a sio:SIO_001121 .
}
dgn-np:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_provenance {
  dgn-np:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_assertion dcterms:description "[This recessively inherited disorder, similar in many respects to Wilson disease, is of particular interest because the canine Atp7b gene, homologous to ATP7B defective in Wilson disease, is not responsible for canine copper toxicosis as has been expected.]. 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:10585777 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP269142.RAuLq60etqEDT0wLwyY2S-Atr-s4YzIjdmoExqDi4zKGU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:48+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}