@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs
> .
@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:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_head
{
this:
np:hasAssertion
dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_assertion
;
np:hasProvenance
dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_provenance
;
np:hasPublicationInfo
dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_assertion
a
np:Assertion
.
dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_provenance
a
np:Provenance
.
dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_assertion
{
miriam-gene:115352
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGNac19b77664381ec3e6207e050fd678a7
sio:SIO_000628
miriam-gene:115352
,
lld:C0026769
;
a
sio:SIO_001122
.
}
dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_provenance
{
dgn-np:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_assertion
dcterms:description
"[An increased susceptibility associated to the -169 T allele was found when MS patients and controls were compared, supporting the role of the FcRL3 locus in MS predisposition and therefore extending the evidence of its general influence on autoimmunity.]. 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:17617473
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP67068.RAsbODbd7TOcB6uCfFvczTywxOwW4TCDyb8bN0_oNoUZs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:32+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" .
}