@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s130_head
{
this:
np:hasAssertion
dgn-np:NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s130_assertion
a
np:Assertion
.
dgn-np:NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s130_provenance
a
np:Provenance
.
dgn-np:NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s130_assertion
{
miriam-gene:596
a
ncit:C16612
.
lld:C0024305
a
ncit:C7057
.
dgn-gda:DGNc222b0dd49560b0bc0148b6d0851e023
sio:SIO_000628
miriam-gene:596
,
lld:C0024305
;
a
sio:SIO_001122
.
}
dgn-np:NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s130_provenance
{
dgn-np:NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s130_assertion
dcterms:description
"[We found no support for a role of the studied variants in BCL2, CCND1, or MYC in risk of NHL or subtypes, but we provide further evidence of putative susceptibility loci in TNF and IL10 for specific NHL subtypes.]. 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:20087644
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP81915.RA6r41Poz_D9RJYTWU9J-fZMuOk9wtRKg0oFA69dQDO_s130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:25+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}