@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0
> .
@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:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_head
{
this:
np:hasAssertion
dgn-np:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_assertion
;
np:hasProvenance
dgn-np:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_provenance
;
np:hasPublicationInfo
dgn-np:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_assertion
a
np:Assertion
.
dgn-np:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_provenance
a
np:Provenance
.
dgn-np:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_assertion
{
miriam-gene:10878
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNedf0027ea024bb3b3ed0fc7fe0350403
sio:SIO_000628
miriam-gene:10878
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_provenance
{
dgn-np:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_assertion
dcterms:description
"[These results suggested that the CFHR3-1Δ deletion within the SLE-associated block, but not the previously described exonic SNPs of CFH, might contribute to the development of SLE in EA, AA, and AS, providing new insights into the role of complement regulators in the pathogenesis of SLE.]. 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:21637784
;
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:NP311405.RA8H924mJQ_UI5Iz8quX2TP2XM0xb1la3jJGbL5gA6hr0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:58+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" .
}