@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ
> .
@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:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_head
{
this:
np:hasAssertion
dgn-np:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_assertion
;
np:hasProvenance
dgn-np:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_assertion
a
np:Assertion
.
dgn-np:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_provenance
a
np:Provenance
.
dgn-np:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0086543
a
ncit:C7057
.
dgn-gda:DGNb4c685f4f44eaf9a2834a5818136835d
sio:SIO_000628
miriam-gene:2952
,
lld:C0086543
;
a
sio:SIO_001122
.
}
dgn-np:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_provenance
{
dgn-np:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_assertion
dcterms:description
"[The present meta-analysis suggested that GSTM1 and GSTT1 null genotypes are associated with increased risk for senile cataract in Asian populations but not in Caucasian populations. Given the limited sample size, the finding on GST polymorphisms merits fu]. 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:20574021
;
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:NP137554.RAVIo0pE8DnPdhmk4AKmj26ab8CpJZvxLg0PmP9ImvYTQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:57+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" .
}