@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_head
{
this:
np:hasAssertion
dgn-np:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_assertion
;
np:hasProvenance
dgn-np:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_assertion
a
np:Assertion
.
dgn-np:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_provenance
a
np:Provenance
.
dgn-np:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_assertion
{
miriam-gene:7361
a
ncit:C16612
.
lld:C0008350
a
ncit:C7057
.
dgn-gda:DGN76d8cbb5c1e9311d9fb7c8d05b18754c
sio:SIO_000628
miriam-gene:7361
,
lld:C0008350
;
a
sio:SIO_001121
.
}
dgn-np:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_provenance
{
dgn-np:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_assertion
dcterms:description
"[Both patients developed gallstones; however the father, who had undergone surgery for the removal of stones, had extremely severe intrahepatic cholestasis and, liver biopsy revealed fibrosis and siderosis grade III, leading us to believe that the homozygosity of the UGT1A polymorphism was responsible for the more severe clinical features in the father.]. 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:25153905
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1213526.RAi2UnAxH6mPj3-d7cCGJVL0YEjxOAlC0nrnVsflFFhp0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:56+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}