@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w
> .
@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:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_head
{
this:
np:hasAssertion
dgn-np:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_assertion
;
np:hasProvenance
dgn-np:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_provenance
;
np:hasPublicationInfo
dgn-np:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_assertion
a
np:Assertion
.
dgn-np:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_provenance
a
np:Provenance
.
dgn-np:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN3cfa6da0411f26a1f3d6f49f3d00b7eb
sio:SIO_000628
miriam-gene:133482
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_provenance
{
dgn-np:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_assertion
dcterms:description
"[To determine whether GST M1, GST T1, and the combined GST M1 and GST T1 null genotypes predict individual susceptibility to tacrine hepatotoxicity, 141 patients with mild to moderate Alzheimer's disease treated with tacrine were genotyped.]. 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:10801254
;
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:NP733469.RAJEeCnCrs0_cNrCFbBYvvCDnygfxn4Bz3Nwabt9oLi4w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:25+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" .
}