@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0> .
@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:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_head {
  this: np:hasAssertion dgn-np:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_assertion ;
    np:hasProvenance dgn-np:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_provenance ;
    np:hasPublicationInfo dgn-np:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_assertion a np:Assertion .
  dgn-np:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_provenance a np:Provenance .
  dgn-np:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_assertion {
  miriam-gene:3689 a ncit:C16612 .
  lld:C0021051 a ncit:C7057 .
  dgn-gda:DGNc660c7345643be5976a15d054a36a94c sio:SIO_000628 miriam-gene:3689 , lld:C0021051 ;
    a sio:SIO_001121 .
}
dgn-np:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_provenance {
  dgn-np:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_assertion dcterms:description "[Leukocyte adhesion deficiency type 1 (LAD-1) is a rare, autosomal recessive inherited immunodeficiency disease characterized by recurrent severe bacterial infection, impaired pus formation, poor wound healing, associated with the mutation in the CD18 gene responsible for the ability of the leucocytes to migrate from the blood stream towards the site of inflammation.]. 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:20529581 ;
    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:NP550421.RAfeTpYPkXGOhn5NrjAbT-Ghm06KkjeEo0cO7W0-3AeN0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:32+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" .
}