@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0
> .
@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:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_head
{
this:
np:hasAssertion
dgn-np:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_assertion
;
np:hasProvenance
dgn-np:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_provenance
;
np:hasPublicationInfo
dgn-np:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_assertion
a
np:Assertion
.
dgn-np:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_provenance
a
np:Provenance
.
dgn-np:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_assertion
{
miriam-gene:6347
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN59c23a016b3a4eb3fd0cc173dca400b9
sio:SIO_000628
miriam-gene:6347
,
lld:C0024141
;
a
sio:SIO_001122
.
}
dgn-np:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_provenance
{
dgn-np:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_assertion
dcterms:description
"[ These results suggest that an A/G or G/G genotype may predispose to the development of SLE and further indicate that SLE patients with these genotypes may be at higher risk of developing LN. Moreover, measurement of urinary levels of MCP-1 may be a useful tool for the detection and management of LN.]. 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:15188361
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47450.RA5hEq3WCy-FYXfObyLtJ9MweQt1r8op-uEWSiIXnvnU0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}