@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE> .
@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:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_head {
  this: np:hasAssertion dgn-np:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_assertion ;
    np:hasProvenance dgn-np:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_provenance ;
    np:hasPublicationInfo dgn-np:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_assertion a np:Assertion .
  dgn-np:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_provenance a np:Provenance .
  dgn-np:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_assertion {
  miriam-gene:64581 a ncit:C16612 .
  lld:C0004030 a ncit:C7057 .
  dgn-gda:DGN25664c8c44745aaa4585eccd217e9a6d sio:SIO_000628 miriam-gene:64581 , lld:C0004030 ;
    a sio:SIO_001121 .
}
dgn-np:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_provenance {
  dgn-np:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_assertion dcterms:description "[We found that the presence of the DECTIN1 Y238X polymorphism in either donors or recipients of hematopoietic stem cell transplantation increased susceptibility to aspergillosis, with the risk being highest when the polymorphism was present simultaneously in both donors and recipients (adjusted hazard ratio = 3.9; P = .005).]. 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:20807886 ;
    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:NP927020.RAvCQdgvdKIeOHDpjay13QAPKkWpoiBCI72Haixq8JYCE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:28+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" .
}