@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI> .
@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:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_head {
  this: np:hasAssertion dgn-np:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_assertion;
    np:hasProvenance dgn-np:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_provenance;
    np:hasPublicationInfo dgn-np:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_assertion a np:Assertion .
  
  dgn-np:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_provenance a np:Provenance .
  
  dgn-np:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_assertion {
  miriam-gene:5265 a ncit:C16612 .
  
  lld:C0221757 a ncit:C7057 .
  
  dgn-gda:DGN8c05d06d4c184b618c0985532ef46dee sio:SIO_000628 miriam-gene:5265, lld:C0221757;
    a sio:SIO_001121 .
}

dgn-np:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_provenance {
  dgn-np:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_assertion dcterms:description
      "[Human AAT deficiency will continue to serve as an excellent model for enhancing our current understanding of mechanisms utilized in regulating protein traffic in the ER and in elucidating the pathophysiologic components of AAT-related liver disease.]. 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:1439881;
    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:NP413613.RANsOASg-wHSHd38lRDg44Qxl3tHADUY8ocW1vtUA5DRI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:52+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" .
}