@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4
> .
@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:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_head
{
this:
np:hasAssertion
dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_assertion
;
np:hasProvenance
dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_provenance
;
np:hasPublicationInfo
dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_assertion
a
np:Assertion
.
dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_provenance
a
np:Provenance
.
dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_assertion
{
miriam-gene:3663
a
ncit:C16612
.
lld:C0004364
a
ncit:C7057
.
dgn-gda:DGNa15aa3a6bd0f450d0e7a11a9f641f53a
sio:SIO_000628
miriam-gene:3663
,
lld:C0004364
;
a
sio:SIO_001121
.
}
dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_provenance
{
dgn-np:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_assertion
dcterms:description
"[Functional genetic variants associated with increased IRF5 expression of specific isoforms are associated with systemic lupus erythematosus (SLE) and it is possible that they may also predispose to other autoimmune disorders.]. 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:17557928
;
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:NP664444.RAfUNIsUOBenVPMKTGmv0KtSn-WEUAPbcrEThycxprEj4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:41+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" .
}