@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg> .
@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:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_head {
  this: np:hasAssertion dgn-np:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_assertion;
    np:hasProvenance dgn-np:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_provenance;
    np:hasPublicationInfo dgn-np:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_assertion a np:Assertion .
  
  dgn-np:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_provenance a np:Provenance .
  
  dgn-np:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_assertion {
  miriam-gene:5265 a ncit:C16612 .
  
  lld:C0037274 a ncit:C7057 .
  
  dgn-gda:DGN7c1f665d7e5ff16b0e01195285523e45 sio:SIO_000628 miriam-gene:5265, lld:C0037274;
    a sio:SIO_001121 .
}

dgn-np:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_provenance {
  dgn-np:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_assertion dcterms:description
      "[Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emphysema, liver cirrhosis and, rarely, as the skin disease panniculitis, and is characterized by low serum levels of AAT, the main protease inhibitor (PI) in human serum.]. 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:18565211;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP426140.RA-pRkEiAnmi5VbDYA5VwAKw2hgsSfaEq4mrWKSD6nmNg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:12+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" .
}