@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g> .
@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:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_head {
  this: np:hasAssertion dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_assertion ;
    np:hasProvenance dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_provenance ;
    np:hasPublicationInfo dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_assertion a np:Assertion .
  dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_provenance a np:Provenance .
  dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_assertion {
  miriam-gene:450095 a ncit:C16612 .
  lld:C0036202 a ncit:C7057 .
  dgn-gda:DGNcc43b56d758d7ef034179d9e45180a5c sio:SIO_000628 miriam-gene:450095 , lld:C0036202 ;
    a sio:SIO_001121 .
}
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_provenance {
  dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_assertion dcterms:description "[However, our study identified the allele TNFB*1, detected by the presence of a NCO: I restriction site, as a marker of prolonged clinical course, with the resolution of sarcoidosis being defined as the disappearance of all clinical symptoms, physical signs of active lesions, abnormal chest radiograph findings, and abnormal results of pulmonary function and biochemical tests.]. 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:11243953 ;
    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:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:28+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" .
}