@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug
> .
@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:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_head
{
this:
np:hasAssertion
dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_assertion
;
np:hasProvenance
dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_provenance
;
np:hasPublicationInfo
dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_assertion
a
np:Assertion
.
dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_provenance
a
np:Provenance
.
dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_assertion
{
miriam-gene:2215
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN2814294c08345d2153f503e0da5ea799
sio:SIO_000628
miriam-gene:2215
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_provenance
{
dgn-np:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_assertion
dcterms:description
"[Given the genetic overlap between systemic lupus erythematosus and systemic sclerosis (SSc) and the strong evidence for FCGR3B CN in the pathology of SLE, we hypothesised that FCGR3B gene dosage influences susceptibility to SSc.]. 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:22551723
;
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:NP287207.RArXv2StPQ7wxIlv1V9NIORbpfaPdXo0nKlFfRCR1GFug130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:43+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" .
}