@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs> .
@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:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_head {
  this: np:hasAssertion dgn-np:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_assertion;
    np:hasProvenance dgn-np:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_provenance;
    np:hasPublicationInfo dgn-np:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_assertion a np:Assertion .
  
  dgn-np:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_provenance a np:Provenance .
  
  dgn-np:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_assertion {
  miriam-gene:540 a ncit:C16612 .
  
  lld:C0019202 a ncit:C7057 .
  
  dgn-gda:DGN0b92216339fa149775aceccdbe431e57 sio:SIO_000628 miriam-gene:540, lld:C0019202;
    a sio:SIO_001121 .
}

dgn-np:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_provenance {
  dgn-np:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_assertion dcterms:description
      "[This is the first study covering Turkish Wilson disease patients and control groups for mutation screening in all the coding regions of ATP7B gene by DNA sequencing method and adding five new mutations and one polymorphism into the HUGO Wilson disease mutation database.]. 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:23333878;
    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:NP257183.RAjL-TYTr-AXvVwYPjmavlTlZnUudfAMzszkkkoXFr4Zs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:06+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}