@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw
> .
@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:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_head
{
this:
np:hasAssertion
dgn-np:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_assertion
;
np:hasProvenance
dgn-np:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_provenance
;
np:hasPublicationInfo
dgn-np:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_assertion
a
np:Assertion
.
dgn-np:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_provenance
a
np:Provenance
.
dgn-np:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_assertion
{
miriam-gene:5966
a
ncit:C16612
.
lld:C0024305
a
ncit:C7057
.
dgn-gda:DGNd30134a5c7affe41a548ca4ce7d626c4
sio:SIO_000628
miriam-gene:5966
,
lld:C0024305
;
a
sio:SIO_001122
.
}
dgn-np:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_provenance
{
dgn-np:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_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:NP82271.RA5cIaPFSKNwYELg5AxEjvjNDVeyjhqsUYYuo1CPqvxiw130_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" .
}