@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw
> .
@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:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_head
{
this:
np:hasAssertion
dgn-np:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_assertion
;
np:hasProvenance
dgn-np:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_provenance
;
np:hasPublicationInfo
dgn-np:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_assertion
a
np:Assertion
.
dgn-np:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_provenance
a
np:Provenance
.
dgn-np:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_assertion
{
miriam-gene:8717
a
ncit:C16612
.
lld:C0024305
a
ncit:C7057
.
dgn-gda:DGN94ed53a7f369a9d8c2227db8fc74510e
sio:SIO_000628
miriam-gene:8717
,
lld:C0024305
;
a
sio:SIO_001122
.
}
dgn-np:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_provenance
{
dgn-np:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_assertion
dc: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:NP80199.RAfB5KC93wFChxVzh1ae9w6kp_bypH6XnZ_1i6sCAlZHw130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:39+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}