@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ
> .
@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:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_head
{
this:
np:hasAssertion
dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_assertion
a
np:Assertion
.
dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_provenance
a
np:Provenance
.
dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C3539909
a
ncit:C7057
.
dgn-gda:DGNa6a80cd152ad55d5b7fdeb05b0919834
sio:SIO_000628
miriam-gene:2952
,
lld:C3539909
;
a
sio:SIO_001121
.
}
dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_provenance
{
dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_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
;
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:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_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
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}