@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU
> .
@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:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_head
{
this:
np:hasAssertion
dgn-np:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_assertion
;
np:hasProvenance
dgn-np:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_provenance
;
np:hasPublicationInfo
dgn-np:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_assertion
a
np:Assertion
.
dgn-np:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_provenance
a
np:Provenance
.
dgn-np:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_assertion
{
miriam-gene:2215
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN826de5fe27af986a4a05fb8f002a824f
sio:SIO_000628
miriam-gene:2215
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_provenance
{
dgn-np:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_assertion
dcterms:description
"[Two-locus analyses suggested that both FCGR2B and FCGR3A may contribute to SLE susceptibility, while the previously reported association of FCGR3B was considered to be secondary and derived from strong linkage disequilibrium with FCGR2B.]. 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:12115230
;
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:NP268811.RAR7vmo_O_Vkbcft7RIN2nUX9p8OscT1eubFEGDLghVuU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}