@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A
> .
@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:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_head
{
this:
np:hasAssertion
dgn-np:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_assertion
;
np:hasProvenance
dgn-np:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_provenance
;
np:hasPublicationInfo
dgn-np:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_assertion
a
np:Assertion
.
dgn-np:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_provenance
a
np:Provenance
.
dgn-np:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_assertion
{
miriam-gene:54658
a
ncit:C16612
.
lld:C0017551
a
ncit:C7057
.
dgn-gda:DGN25039ad3699d59393556ee3ce6f27a30
sio:SIO_000628
miriam-gene:54658
,
lld:C0017551
;
a
sio:SIO_001121
.
}
dgn-np:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_provenance
{
dgn-np:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_assertion
dcterms:description
"[Because of the health and therapeutic implications of slightly elevated serum bilirubin concentrations, we will discuss the recent prospective studies on cardiovascular risk in individuals with Gilbert syndrome (GS) as well as those with the UGT1A1*28 allele.]. 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:18343383
;
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:NP156028.RARlB3Zq2SCpbSmED-NEXiFQ3bUDf6S5RJ-nvsoyhj98A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:24+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" .
}