@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec> .
@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:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_head {
  this: np:hasAssertion dgn-np:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_assertion ;
    np:hasProvenance dgn-np:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_provenance ;
    np:hasPublicationInfo dgn-np:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_assertion a np:Assertion .
  dgn-np:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_provenance a np:Provenance .
  dgn-np:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_assertion {
  miriam-gene:5265 a ncit:C16612 .
  lld:C0042164 a ncit:C7057 .
  dgn-gda:DGN4f1b580fdd7f40abf78acc912ef5736c sio:SIO_000628 miriam-gene:5265 , lld:C0042164 ;
    a sio:SIO_001121 .
}
dgn-np:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_provenance {
  dgn-np:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_assertion dcterms:description "[Recent evidence has linked some mildly deficient phenotypes of Pi with a variety of chronic immunologic and inflammatory disorders, such as rheumatoid arthritis, juvenile chronic arthritis, systemic lupus erythematosus, ankylosing spondylitis, uveitis, asthma and fibrosing alveolitis, in addition to the well recognised association of severe deficiency with emphysema and chronic 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:6968557 ;
    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:NP275024.RAirQ6qGwEGZ5l4iEiUDfAX_IF_B3wrCC_Kv6qorqgyec130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:35+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" .
}