@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc
> .
@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:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_head
{
this:
np:hasAssertion
dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_assertion
;
np:hasProvenance
dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_provenance
;
np:hasPublicationInfo
dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_provenance
a
np:Provenance
.
dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_assertion
{
miriam-gene:26188
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN119af3b91427e17b4fcd74e5446f0fad
sio:SIO_000628
miriam-gene:26188
,
lld:C0003873
;
a
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.
}
dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_provenance
{
dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_assertion
dcterms:description
"[Among the 120 RA patients being heterozygous in the promoter region of Fas_-670A/G (OR 1.42,CI 0.92-1.52, P = 0.18) and FasL_-844C/T (OR 1.42, CI 0.92-1.52, P = 0.18) and homozygous in the minor allele for FasLIVS2nt_124G/G (OR 1.43, CI 0.76-1.81, P = 0.7), the frequency of these polymorphisms is higher in the cases than in controls and the elevated risk of RA were observed when the patient compared with controls, although this is not statistically significant.]. 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:21879377
;
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:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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
<
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> , <
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" .
}