@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI
> .
@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:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_head
{
this:
np:hasAssertion
dgn-np:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_assertion
;
np:hasProvenance
dgn-np:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_provenance
;
np:hasPublicationInfo
dgn-np:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_assertion
a
np:Assertion
.
dgn-np:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_provenance
a
np:Provenance
.
dgn-np:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_assertion
{
miriam-gene:1147
a
ncit:C16612
.
lld:C0024305
a
ncit:C7057
.
dgn-gda:DGN74140960b3c88cf51a1af067e32bc30a
sio:SIO_000628
miriam-gene:1147
,
lld:C0024305
;
a
sio:SIO_001122
.
}
dgn-np:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_provenance
{
dgn-np:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_assertion
dcterms: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:NP77688.RAwdFzvZY6xwZ_ReLsUVMCjbRWhhGO0i0vLyksQuR_gnI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:38+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" .
}