@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY
> .
@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:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_head
{
this:
np:hasAssertion
dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_assertion
;
np:hasProvenance
dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_provenance
;
np:hasPublicationInfo
dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_assertion
a
np:Assertion
.
dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_provenance
a
np:Provenance
.
dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_assertion
{
miriam-gene:5243
a
ncit:C16612
.
lld:C0151746
a
ncit:C7057
.
dgn-gda:DGN5b369042aae77bbf5a6585b4248c838e
sio:SIO_000628
miriam-gene:5243
,
lld:C0151746
;
a
sio:SIO_001122
.
}
dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_provenance
{
dgn-np:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_assertion
dcterms:description
"[ Based on these results, we conclude that homozygosity for the ABCB1 2677T (S893) allele is associated with reduced risk of chronic renal dysfunction among liver transplantation patients receiving an immunosuppressive regimen containing CNIs.]. 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:14583679
;
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:NP49796.RAjVDJVOwqVlcSwNtwyn6jhiT8Xwqb2iPQSfJz61gV5eY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}