@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg
> .
@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:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_head
{
this:
np:hasAssertion
dgn-np:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_assertion
;
np:hasProvenance
dgn-np:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_provenance
;
np:hasPublicationInfo
dgn-np:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_assertion
a
np:Assertion
.
dgn-np:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_provenance
a
np:Provenance
.
dgn-np:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_assertion
{
miriam-gene:7361
a
ncit:C16612
.
lld:C0020433
a
ncit:C7057
.
dgn-gda:DGN025545b4eced97bab762e729daffa913
sio:SIO_000628
miriam-gene:7361
,
lld:C0020433
;
a
sio:SIO_001121
.
}
dgn-np:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_provenance
{
dgn-np:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_assertion
dcterms:description
"[We show that the combined effect of an increased bilirubin load caused by dyserythropoiesis in CDA II and decreased bilirubin conjugation caused by reduced expression of uridine diphosphate glucuronosyl transferase (UGT1A) would increase the risk of hyperbilirubinemia (P <.005) and gallstone formation (chi(2): P <.]. 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:10753261
;
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:NP389088.RAYMmjBeY_GqHB-bh3nIUZzSul5oK47RJ1cR9d51lo9Sg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}