@prefix semsc: <
http://semanticscience.org/resource/
> .
@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@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 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:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_head
{
this:
np:hasAssertion
dgn-np:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_assertion
;
np:hasProvenance
dgn-np:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_provenance
;
np:hasPublicationInfo
dgn-np:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_assertion
a
np:Assertion
.
dgn-np:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_provenance
a
np:Provenance
.
dgn-np:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGN5f995d2cea1ebabfa843b6e87625aafe
semsc:SIO_000628
miriam-gene:2952
,
lld:C0024623
;
a
semsc:SIO_001121
.
}
dgn-np:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_provenance
{
dgn-np:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_assertion
dct:description
"[A case-control study was performed in 303 subjects (108 GC and 195 healthy controls) to analyze the association of polymorphisms in GSTM1, GSTT1, GSTP1, GSTM3, CYP1A1, and CYP2E1 genes in susceptibility to GC in Kashmir Valley.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
semsc:SIO_000772
miriam-pubmed:19521675
;
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:NP209326.RADsH2ilfnVttRFh9WAMbGdsfc9CFVuAKfTHJPZAVTG-c130_publicationInfo
{
this:
dct:created
"2014-10-02T12:33:55+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
semsc:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}