@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g
> .
@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:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_head
{
this:
np:hasAssertion
dgn-np:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_assertion
;
np:hasProvenance
dgn-np:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_provenance
;
np:hasPublicationInfo
dgn-np:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_assertion
a
np:Assertion
.
dgn-np:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_provenance
a
np:Provenance
.
dgn-np:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGNab9a0096a91f55566538488460178a64
sio:SIO_000628
miriam-gene:133482
,
lld:C1140680
;
a
sio:SIO_001121
.
}
dgn-np:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_provenance
{
dgn-np:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_assertion
dcterms:description
"[To assess the role of GST gene variants in ovarian cancer development, we screened 285 epithelial ovarian cancer cases and 299 unaffected controls for the GSTT1 deletion (null) variant, the GSTM1 deletion (null) variant and the GSTP1 codon 104 A-->G Ile-->Val amino acid substitution variant.]. 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:11159743
;
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:NP434497.RAu2cCBpcZs6b42xxYor3Xla2PMIosoib90RjFf_gsK2g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:17+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" .
}