@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0> .
@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 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:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_head {
  this: np:hasAssertion dgn-np:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_assertion ;
    np:hasProvenance dgn-np:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_provenance ;
    np:hasPublicationInfo dgn-np:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_assertion a np:Assertion .
  dgn-np:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_provenance a np:Provenance .
  dgn-np:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_assertion {
  miriam-gene:3106 a ncit:C16612 .
  lld:C0018133 a ncit:C7057 .
  dgn-gda:DGNa82c5b9d2590b492bedf2bb9ec434c60 sio:SIO_000628 miriam-gene:3106 , lld:C0018133 ;
    a sio:SIO_001122 .
}
dgn-np:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_provenance {
  dgn-np:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_assertion dct:description "[In conclusion, utilization of modeling HLA molecular three-dimension can predict the severe aGVHD after UCBT quickly, simply and accurately. It provides scientific basis in choosing a optimal cord blood donor to avoid severe aGVHD for physicians and the cord blood banks. And it is instructive too to direct the application of immunosuppressive agents after transplantation in clinic.]. 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:15228651 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP58267.RA-_pm4zZejj0jHIMEl4uA7ILbRJ29awMxldsEBpHwUK0130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}