@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw> .
@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:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_head {
  this: np:hasAssertion dgn-np:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_assertion;
    np:hasProvenance dgn-np:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_provenance;
    np:hasPublicationInfo dgn-np:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_assertion a np:Assertion .
  
  dgn-np:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_provenance a np:Provenance .
  
  dgn-np:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_assertion {
  miriam-gene:5265 a ncit:C16612 .
  
  lld:C0221757 a ncit:C7057 .
  
  dgn-gda:DGN809cf9b6d3e62a73049c68d86ef21b5c sio:SIO_000628 miriam-gene:5265, lld:C0221757;
    a sio:SIO_001122 .
}

dgn-np:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_provenance {
  dgn-np:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_assertion dcterms:description
      "[Alpha-1-antitrypsin deficiency (AAT deficiency) is one of the most common serious hereditary disorders in the world, as its affects all major racial subgroups worldwide, and there are an estimated 120.5 million carriers and deficient subjects worldwide.]. 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:14616761;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP52029.RACACo5uYtUp7oTA6v9PtRhbpj5F3detnBY62gwU-juWw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}