@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_head
{
this:
np:hasAssertion
dgn-np:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_assertion
;
np:hasProvenance
dgn-np:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_provenance
;
np:hasPublicationInfo
dgn-np:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_assertion
a
np:Assertion
.
dgn-np:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_provenance
a
np:Provenance
.
dgn-np:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_assertion
{
miriam-gene:2215
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNecb051e2b34b805cd8f0f2ab482f851c
sio:SIO_000628
miriam-gene:2215
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_provenance
{
dgn-np:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_assertion
dcterms:description
"[The variable gene copy number of FCGR3B is found to be involved in the impaired clearance of immune complexes, which significantly contribute to the pathogenesis of several autoimmune diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), type-1 diabetes and others.]. 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:25428402
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1240576.RAFQfhYUOQ0-GDXEbLmhb3m0CxF16ug31v1Sf-HXue2Ks130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:08+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}