@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I
> .
@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 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:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_head
{
this:
np:hasAssertion
dgn-np:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_assertion
;
np:hasProvenance
dgn-np:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_provenance
;
np:hasPublicationInfo
dgn-np:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_assertion
a
np:Assertion
.
dgn-np:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_provenance
a
np:Provenance
.
dgn-np:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_assertion
{
miriam-gene:8737
a
ncit:C16612
.
lld:C0024305
a
ncit:C7057
.
dgn-gda:DGN0fbb18054c4d1826912f686446b48938
sio:SIO_000628
miriam-gene:8737
,
lld:C0024305
;
a
sio:SIO_001122
.
}
dgn-np:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_provenance
{
dgn-np:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_assertion
dct:description
"[we provide additional evidence for the role of genetic variation in TNF and LTA SNPs and haplotypes with risk of NHL and also provide some of the first preliminary evidence for an association of genetic variation in NFKB1, a downstream target of TNF sig]. 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:18990758
;
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:NP82132.RAxmSDg2Yg4K1vuf9j38dxC2rrr1xbBqC3V1TQs4QwV8I130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:40+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}