@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g
> .
@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:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_head
{
this:
np:hasAssertion
dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_assertion
;
np:hasProvenance
dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_provenance
;
np:hasPublicationInfo
dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_assertion
a
np:Assertion
.
dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_provenance
a
np:Provenance
.
dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0086543
a
ncit:C7057
.
dgn-gda:DGN409dc803914b5ea98ebdf083feb298ee
sio:SIO_000628
miriam-gene:2944
,
lld:C0086543
;
a
sio:SIO_001122
.
}
dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_provenance
{
dgn-np:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_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 further investigation.]. 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-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP86955.RAWCsZMf5AwxJD3jOWhlVAlnari6fx7PCuJ0iqCcZaE8g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:43+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" .
}