@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI
> .
@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:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_head
{
this:
np:hasAssertion
dgn-np:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_assertion
;
np:hasProvenance
dgn-np:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_provenance
;
np:hasPublicationInfo
dgn-np:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_assertion
a
np:Assertion
.
dgn-np:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_provenance
a
np:Provenance
.
dgn-np:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_assertion
{
miriam-gene:414062
a
ncit:C16612
.
lld:C0151449
a
ncit:C7057
.
dgn-gda:DGN26374a2ebab5064f3c3194fdb404150e
sio:SIO_000628
miriam-gene:414062
,
lld:C0151449
;
a
sio:SIO_001121
.
}
dgn-np:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_provenance
{
dgn-np:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_assertion
dcterms:description
"[In a cross-sectional study of 774 subjects, we estimated FCGR3B and CCL3L1 gene copy number in 146, 158 and 61 subjects with systemic lupus erythematosus (SLE), rheumatoid arthritis (RA) and primary Sjögren's syndrome (SS), respectively, and 409 healthy controls.]. 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:19741716
;
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:NP534468.RAjqoIvSUWFHn0Ai2DS8agAdr0rWj6lptDQ3H-F7GEhoI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:22+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" .
}