@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek> .
@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:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_head {
   this: np:hasAssertion dgn-np:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_assertion ;
    np:hasProvenance dgn-np:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_provenance ;
    np:hasPublicationInfo dgn-np:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_assertion a np:Assertion .
  dgn-np:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_provenance a np:Provenance .
  dgn-np:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_assertion {
   miriam-gene:475 a ncit:C16612 .
  lld:C0302332 a ncit:C7057 .
  dgn-gda:DGNff351f425dfeeff86cad238309b01f00 sio:SIO_000628 miriam-gene:475 , lld:C0302332 ;
    a sio:SIO_001121 .
}
dgn-np:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_provenance {
   dgn-np:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_assertion dcterms:description "[Recently, the gene underlying Wilson disease (ATP7B) as well as copper transport genes hCTR1, hCTR2 and ATOX1 have been excluded as candidates for NICC in man and copper toxicosis in Bedlington terriers.]. 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:10425268 ;
    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:NP258840.RAGroOWwHFbv9S7jpG1pXAKG4knJL6WG27afHBr3a8Fek130_publicationInfo {
   this: dcterms:created "2016-05-13T12:43:43+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" .
}