@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk
> .
@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:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_head
{
this:
np:hasAssertion
dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_assertion
;
np:hasProvenance
dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_provenance
;
np:hasPublicationInfo
dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_assertion
a
np:Assertion
.
dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_provenance
a
np:Provenance
.
dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_assertion
{
miriam-gene:2209
a
ncit:C16612
.
lld:C0151449
a
ncit:C7057
.
dgn-gda:DGN09b74f4e2e1a3a19e052a350eff761d5
sio:SIO_000628
miriam-gene:2209
,
lld:C0151449
;
a
sio:SIO_001121
.
}
dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_provenance
{
dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_assertion
dcterms:description
"[The lack of association of pSS with Fcγ receptor gene variants indicates that defective immune complex clearance may not be as important in pSS pathogenesis as in SLE, and may point to important differences between SLE and pSS.]. 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:23552400
;
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:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:21+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" .
}