@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" .
}