@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1248634.RArC_LJHzS8waTazt0guOI5G4eEI9Y7GL_4gVb9yknIsY
> .
@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/
> .
dgn-np:NP1248634.RArC_LJHzS8waTazt0guOI5G4eEI9Y7GL_4gVb9yknIsY130_head
{
this:
np:hasAssertion
dgn-np:NP1248634.RArC_LJHzS8waTazt0guOI5G4eEI9Y7GL_4gVb9yknIsY130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
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;
a
np:Nanopublication
.
dgn-np:NP1248634.RArC_LJHzS8waTazt0guOI5G4eEI9Y7GL_4gVb9yknIsY130_assertion
a
np:Assertion
.
dgn-np:NP1248634.RArC_LJHzS8waTazt0guOI5G4eEI9Y7GL_4gVb9yknIsY130_provenance
a
np:Provenance
.
dgn-np:NP1248634.RArC_LJHzS8waTazt0guOI5G4eEI9Y7GL_4gVb9yknIsY130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP1248634.RArC_LJHzS8waTazt0guOI5G4eEI9Y7GL_4gVb9yknIsY130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C3539909
a
ncit:C7057
.
dgn-gda:DGNf9a1a7fda67ab9c8742d3c387e44d423
sio:SIO_000628
miriam-gene:133482
,
lld:C3539909
;
a
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.
}
dgn-np:NP1248634.RArC_LJHzS8waTazt0guOI5G4eEI9Y7GL_4gVb9yknIsY130_provenance
{
dgn-np:NP1248634.RArC_LJHzS8waTazt0guOI5G4eEI9Y7GL_4gVb9yknIsY130_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 ;
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dgn-void:source_evidence_literature
;
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 .
}
dgn-np:NP1248634.RArC_LJHzS8waTazt0guOI5G4eEI9Y7GL_4gVb9yknIsY130_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
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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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pav:version
"v4.0.0" .
}