@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg
> .
@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:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_head
{
this:
np:hasAssertion
dgn-np:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_assertion
;
np:hasProvenance
dgn-np:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_provenance
;
np:hasPublicationInfo
dgn-np:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_assertion
a
np:Assertion
.
dgn-np:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_provenance
a
np:Provenance
.
dgn-np:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_assertion
{
miriam-gene:2947
a
ncit:C16612
.
lld:C0016978
a
ncit:C7057
.
dgn-gda:DGN6921dcfdd8de350648cccb2cc66a5ca3
sio:SIO_000628
miriam-gene:2947
,
lld:C0016978
;
a
sio:SIO_001122
.
}
dgn-np:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_provenance
{
dgn-np:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_assertion
dcterms:description
"[To find out the association of GST variants with risk of gallbladder cancer, the distribution of polymorphisms in the GST family of genes (GSTT1, GSTM1, GSTP1, and GSTM3) were studied in 106 cancer patients and 201 healthy controls.]. 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:16760134
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP145785.RAJ3Y1RE5eNgVfLT7WO_ujHFImxzc95kRb3XpwpGFIqsg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:16+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" .
}