@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw
> .
@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:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_head
{
this:
np:hasAssertion
dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_assertion
;
np:hasProvenance
dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_provenance
;
np:hasPublicationInfo
dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_assertion
a
np:Assertion
.
dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_provenance
a
np:Provenance
.
dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_assertion
{
miriam-gene:3106
a
ncit:C16612
.
lld:C0018133
a
ncit:C7057
.
dgn-gda:DGNc0f89e6f37fe45f1b64170dd9984b0be
sio:SIO_000628
miriam-gene:3106
,
lld:C0018133
;
a
sio:SIO_001122
.
}
dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_provenance
{
dgn-np:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_assertion
dcterms:description
"[Overall, these results suggest that the matching of microsatellite polymorphisms within the HLA region, especially the ones farthest from the classical HLA loci, was not useful indicator for the outcome of HSC transplantation from unrelated donors. In this regard, the future determination of the genome-wide microsatellite genotypes in HLA-matched donor-recipient pairs, outside the MHC, may be a better possibility for identifying minor histocompatibility genes in linkage disequilibria with microsatellites as potential predictive markers for the occurrence of acute GVHD and survival rate in HSC transplantation.]. 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:15009808
;
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:NP58268.RAfave8pZMb3YMRZv85bpZiKdYB7x-uMW2pbxR-QdkcGw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}