@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw
> .
@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:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_head
{
this:
np:hasAssertion
dgn-np:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_assertion
;
np:hasProvenance
dgn-np:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_provenance
;
np:hasPublicationInfo
dgn-np:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_assertion
a
np:Assertion
.
dgn-np:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_provenance
a
np:Provenance
.
dgn-np:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_assertion
{
miriam-gene:2950
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGN23b8ebdbc5b085de16a5021da14346dd
sio:SIO_000628
miriam-gene:2950
,
lld:C0017601
;
a
sio:SIO_001121
.
}
dgn-np:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_provenance
{
dgn-np:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_assertion
dcterms:description
"[GSTM1, GSTP1, and GSTT1 gene polymorphisms were not different among exfoliation syndrome patients, with or without glaucoma, and the controls therefore GSTM1, GSTP1, and GSTT1 gene polymorphisms did not seem to be associated with the risk of development of exfoliation syndrome.]. 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:16020292
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP664013.RACNtlp04V0ehG-k23GC_QnjQHe9ls9MM7VXaGja1qKYw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:41+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" .
}