@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc
> .
@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:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_head
{
this:
np:hasAssertion
dgn-np:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_assertion
;
np:hasProvenance
dgn-np:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_provenance
;
np:hasPublicationInfo
dgn-np:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_assertion
a
np:Assertion
.
dgn-np:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_provenance
a
np:Provenance
.
dgn-np:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_assertion
{
miriam-gene:373156
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN35d9c905a99651dbbe19a3d78e81ac0b
sio:SIO_000628
miriam-gene:373156
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_provenance
{
dgn-np:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_assertion
dcterms:description
"[To screen genetic variations in GST for an effect on the onset age (OA) of PD, we typed seven common genetic polymorphisms in five GST isoenzymes, M1, M3, P1, T1, and Z1, in 36 affected individuals of Italian or Greek origin with the alpha-synuclein A53T (PARK1) mutation.]. 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:17034008
;
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:NP753760.RA1rk7fgOtfgaXkwok7g--9aOkr1r8LgclkWlZ2fyoNuc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}