@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18> .
@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 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:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_head {
  this: np:hasAssertion dgn-np:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_assertion;
    np:hasProvenance dgn-np:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_provenance;
    np:hasPublicationInfo dgn-np:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_assertion a np:Assertion .
  
  dgn-np:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_provenance a np:Provenance .
  
  dgn-np:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_publicationInfo a np:PublicationInfo .
}

dgn-np:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_assertion {
  miriam-gene:540 a ncit:C16612 .
  
  lld:C0019202 a ncit:C7057 .
  
  dgn-gda:DGNaed4fa985098c569bf35f2d8beef6096 sio:SIO_000628 miriam-gene:540, lld:C0019202;
    a sio:SIO_001122 .
}

dgn-np:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_provenance {
  dgn-np:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_assertion dcterms:description
      "[In this study, we report the further results of an ongoing project on the delineation of the spectrum of mutations on the ATP7B gene in Wilson disease (WD) patients of Greek origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:11216666;
    prov:wasDerivedFrom dgn-void:uniprot-2016;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  
  dgn-void:uniprot-2016 pav:importedOn "2016-01-25"^^xsd:date .
}

dgn-np:NP1286.RAoUPhjRAJUgI6TlBS8UZD2w_7EMDyEe9TZ-hq-3aGS18130_publicationInfo {
  this: dcterms:created "2016-05-13T12:41:50+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 orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}