@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk
> .
@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:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_head
{
this:
np:hasAssertion
dgn-np:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_assertion
;
np:hasProvenance
dgn-np:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_provenance
;
np:hasPublicationInfo
dgn-np:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_assertion
a
np:Assertion
.
dgn-np:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_provenance
a
np:Provenance
.
dgn-np:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_assertion
{
miriam-gene:930
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN8f6742f2485c20a0db70747d183ed02c
sio:SIO_000628
miriam-gene:930
,
lld:C0024141
;
a
sio:SIO_001122
.
}
dgn-np:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_provenance
{
dgn-np:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_assertion
dcterms:description
"[These results suggested that either the slight reduction in the CD19 mRNA level associated with the elongation of GT repeat, or an allele of another locus in linkage disequilibrium with CD19 (GT)(15-18), may be associated with susceptibility to SLE in Japanese.]. 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:12215898
;
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:NP47136.RAzz302Qbql63GKeKarPZ2-4VVt4GyGzqwrVPEUeTVCLk130_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" .
}