@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM
> .
@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:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_head
{
this:
np:hasAssertion
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_assertion
;
np:hasProvenance
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_provenance
;
np:hasPublicationInfo
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_assertion
a
np:Assertion
.
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_provenance
a
np:Provenance
.
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_assertion
{
miriam-gene:2212
a
ncit:C16612
.
lld:C0024305
a
ncit:C7057
.
dgn-gda:DGNeec5223fb61c2da979105412d026ac42
sio:SIO_000628
miriam-gene:2212
,
lld:C0024305
;
a
sio:SIO_001122
.
}
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_provenance
{
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_assertion
dcterms:description
"[common variants in genes influencing proinflammatory and innate immune responses were associated with non-Hodgkin lymphoma risk overall and their effects could vary by subtype. Our results require replication but potentially provide important clues for investigating common genetic variants as susceptibility factors and in disease outcomes, treatment responses, and immunotherapy targets. (Cancer Res 2006; 66(19): 9771-80).]. 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:17018637
;
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:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}