@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_head
{
this:
np:hasAssertion
dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_assertion
;
np:hasProvenance
dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_provenance
;
np:hasPublicationInfo
dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_assertion
a
np:Assertion
.
dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_provenance
a
np:Provenance
.
dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_assertion
{
miriam-gene:9446
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN12cefb73dce6f3c209900145c366832e
sio:SIO_000628
miriam-gene:9446
,
lld:C0020179
;
a
sio:SIO_001122
.
}
dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_provenance
{
dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_assertion
dcterms:description
"[After genotyping GSTO1 and GSTO2 polymorphisms, firstly there was no statistically significant difference in AO for HD patients, as well as secondly for HD patients vs. controls concerning, both, genotype and allele frequencies, respectively.]. 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:15040808
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:08+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}