@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU
> .
@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:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_head
{
this:
np:hasAssertion
dgn-np:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_assertion
;
np:hasProvenance
dgn-np:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_provenance
;
np:hasPublicationInfo
dgn-np:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_assertion
a
np:Assertion
.
dgn-np:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_provenance
a
np:Provenance
.
dgn-np:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_assertion
{
miriam-gene:10318
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNb416ce06f825e82e905a37eacbb3d53c
sio:SIO_000628
miriam-gene:10318
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_provenance
{
dgn-np:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_assertion
dcterms:description
"[TNIP1 is a shared SLE susceptibility gene in the Caucasian and Asian populations, but the genetic contribution appeared to be greater in the Japanese and Chinese populations because of the higher risk allele frequency.]. 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:20849588
;
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:NP275690.RA02Y8e4YaDqv6fWcgK9gZ-_F27E3mMX7iGkGVxDea9lU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}