@prefix this: <
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> .
@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/v4.0.0/void/
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1248637.RA07MEBWrtPTpkGhKExvjyHzpon1V9G637DA9U7TxIRsQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1248637.RA07MEBWrtPTpkGhKExvjyHzpon1V9G637DA9U7TxIRsQ130_assertion
a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP1248637.RA07MEBWrtPTpkGhKExvjyHzpon1V9G637DA9U7TxIRsQ130_publicationInfo
a
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.
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dgn-np:NP1248637.RA07MEBWrtPTpkGhKExvjyHzpon1V9G637DA9U7TxIRsQ130_assertion
{
miriam-gene:2950
a
ncit:C16612
.
lld:C3539909
a
ncit:C7057
.
dgn-gda:DGN4c83d85c572d08255d939149f7697445
sio:SIO_000628
miriam-gene:2950
,
lld:C3539909
;
a
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.
}
dgn-np:NP1248637.RA07MEBWrtPTpkGhKExvjyHzpon1V9G637DA9U7TxIRsQ130_provenance
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dgn-np:NP1248637.RA07MEBWrtPTpkGhKExvjyHzpon1V9G637DA9U7TxIRsQ130_assertion
dcterms:description
"[In analyzing GSTM1, GSTT1, and GSTP1 sequence variation, we observed other common functional variants that may be candidates for associated studies of diseases related to GST genes (e.g., cancer, cardiovascular disease, and allergy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:25515186
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP1248637.RA07MEBWrtPTpkGhKExvjyHzpon1V9G637DA9U7TxIRsQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:12+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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
"v4.0.0.0" .
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"v4.0.0" .
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