@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU> .
@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:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_head {
  this: np:hasAssertion dgn-np:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_assertion ;
    np:hasProvenance dgn-np:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_provenance ;
    np:hasPublicationInfo dgn-np:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_assertion a np:Assertion .
  dgn-np:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_provenance a np:Provenance .
  dgn-np:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_assertion {
  miriam-gene:260431 a ncit:C16612 .
  lld:C0004096 a ncit:C7057 .
  dgn-gda:DGN07018b15426b832205d96c994b6dc0c5 sio:SIO_000628 miriam-gene:260431 , lld:C0004096 ;
    a sio:SIO_001121 .
}
dgn-np:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_provenance {
  dgn-np:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_assertion dcterms:description "[The most frequent causes of missing the diagnosis are (1) atypical clinical presentation, (2) misconceptions about age of onset of childhood asthma, and (3) the coexistence of another chronic respiratory illness that may have a more dramatic clinical picture and constitute a `red herring.` It is fascinating to speculate on the similarities and differences between classical asthma (which has a usually completely reversible obstruction) and the hyperreactivity and partial reversibility of chronic inflammatory diseases like COPD or CF.]. 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:3896051 ;
    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:NP416758.RAv8phRhoJfnPpe6zVx2pkXPx292rqzL2MpqBOLNTRQJU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:07+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" .
}