@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw
> .
@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:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_head
{
this:
np:hasAssertion
dgn-np:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_assertion
;
np:hasProvenance
dgn-np:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_provenance
;
np:hasPublicationInfo
dgn-np:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_assertion
a
np:Assertion
.
dgn-np:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_provenance
a
np:Provenance
.
dgn-np:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_assertion
{
miriam-gene:2523
a
ncit:C16612
.
lld:C0018133
a
ncit:C7057
.
dgn-gda:DGN7d14e9f3c101469e558961cc95bc91ea
sio:SIO_000628
miriam-gene:2523
,
lld:C0018133
;
a
sio:SIO_001121
.
}
dgn-np:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_provenance
{
dgn-np:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_assertion
dcterms:description
"[In order to determine whether matching/mismatching for microsatellite polymorphism provides useful information on acute graft-vs-host disease (GVHD), survival, and leukemia relapse in hematopoietic stem cell (HSC) transplantation, we genotyped for polymorphisms at 13 microsatellite loci within the major histocompatibility complex (MHC) of 100 unrelated HSC transplant donor-recipient pairs who were matched at five classical human leukocyte antigen (HLA) loci.]. 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: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:NP703347.RAv0PBnt-aj13I98xIS1JvY-Apmd4thRvSl4amH9HKqhw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:07+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" .
}