@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE
> .
@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:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_head
{
this:
np:hasAssertion
dgn-np:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_assertion
;
np:hasProvenance
dgn-np:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_provenance
;
np:hasPublicationInfo
dgn-np:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_assertion
a
np:Assertion
.
dgn-np:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_provenance
a
np:Provenance
.
dgn-np:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_assertion
{
miriam-gene:54658
a
ncit:C16612
.
lld:C0022353
a
ncit:C7057
.
dgn-gda:DGN542322602f408273b433682f90268b3a
sio:SIO_000628
miriam-gene:54658
,
lld:C0022353
;
a
sio:SIO_001121
.
}
dgn-np:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_provenance
{
dgn-np:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_assertion
dcterms:description
"[Mutation of the UGT1A1 gene, glycine to arginine at codon 71 (G71R), is related to the development of neonatal jaundice in East Asian populations but the frequency of this mutation is rare among Caucasian populations.]. 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:20528217
;
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:NP454476.RAXb_7XgaUEfEyN8G6Z3JpvDBliwlzNqDX14L7EWG0IyE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:31+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" .
}