@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk
> .
@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:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_head
{
this:
np:hasAssertion
dgn-np:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_assertion
;
np:hasProvenance
dgn-np:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_provenance
;
np:hasPublicationInfo
dgn-np:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_assertion
a
np:Assertion
.
dgn-np:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_provenance
a
np:Provenance
.
dgn-np:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_assertion
{
miriam-gene:3809
a
ncit:C16612
.
lld:C0856825
a
ncit:C7057
.
dgn-gda:DGNc79b953aa79adace34f662e36a763b08
sio:SIO_000628
miriam-gene:3809
,
lld:C0856825
;
a
sio:SIO_001121
.
}
dgn-np:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_provenance
{
dgn-np:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_assertion
dcterms:description
"[After controlling for other transplant factors, including donor type (sibling or unrelated), transplant source (bone marrow or peripheral blood stem cells), and acute GVHD grade, regression analysis of elevated KIR gene expression found an association for both KIR2DS2 and KIR2DS4, with a 7-fold increase in risk for CMV reactivation.]. 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:21596150
;
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:NP271258.RAedAPz5hJzSlWUKqGpapisNZ1hSF1dDxVurqKILSnCBk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:31+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" .
}