@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M
> .
@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:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_head
{
this:
np:hasAssertion
dgn-np:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_assertion
;
np:hasProvenance
dgn-np:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_provenance
;
np:hasPublicationInfo
dgn-np:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_assertion
a
np:Assertion
.
dgn-np:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_provenance
a
np:Provenance
.
dgn-np:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0079744
a
ncit:C7057
.
dgn-gda:DGN528e63444fc459e9593d352a1e4a8d2f
sio:SIO_000628
miriam-gene:2944
,
lld:C0079744
;
a
sio:SIO_001121
.
}
dgn-np:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_provenance
{
dgn-np:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_assertion
dcterms:description
"[Further studies on the functional consequences of GSTT1 and GSTM1 genetic polymorphisms would pave the way to declare their role in the pathogenesis of DLBCL or as possible predictors for response to therapy.]. 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:22484853
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP436550.RAkD27i-DxUp9y1UPxktenX1n0xSsrtsZj-lWk1mdrz3M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}