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http://rdf.disgenet.org/nanopublications.trig#NP794120.RAwGc_kl2YQYkKOkiyUFBl7FXUNDwfeBvUFqi5xzcE2Dw
> .
@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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
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dgn-np:NP794120.RAwGc_kl2YQYkKOkiyUFBl7FXUNDwfeBvUFqi5xzcE2Dw130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP794120.RAwGc_kl2YQYkKOkiyUFBl7FXUNDwfeBvUFqi5xzcE2Dw130_provenance
a
np:Provenance
.
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np:PublicationInfo
.
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{
miriam-gene:100653366
a
ncit:C16612
.
lld:C0036646
a
ncit:C7057
.
dgn-gda:DGN32d8bbca49ff63e4167615c3186d9e4f
sio:SIO_000628
miriam-gene:100653366
,
lld:C0036646
;
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.
}
dgn-np:NP794120.RAwGc_kl2YQYkKOkiyUFBl7FXUNDwfeBvUFqi5xzcE2Dw130_provenance
{
dgn-np:NP794120.RAwGc_kl2YQYkKOkiyUFBl7FXUNDwfeBvUFqi5xzcE2Dw130_assertion
dcterms:description
"[We compared the prevalence of GSTT1 and GSTM1 deletion genotypes, which were determined by multiplex polymerase chain reaction, in 455 patients with ARCs (108 with nuclear (NC), 105 with cortical (CC), 96 with posterior subcapsular, (PSC) and 146 with mixed type (MT)) and 205 age and sex matched 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:22446016
;
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:NP794120.RAwGc_kl2YQYkKOkiyUFBl7FXUNDwfeBvUFqi5xzcE2Dw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+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
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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pav:version
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}