@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs
> .
@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:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_head
{
this:
np:hasAssertion
dgn-np:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_assertion
;
np:hasProvenance
dgn-np:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_provenance
;
np:hasPublicationInfo
dgn-np:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_assertion
a
np:Assertion
.
dgn-np:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_provenance
a
np:Provenance
.
dgn-np:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_assertion
{
miriam-gene:1103
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN16c692fa7131b0679958fdf94b73be5f
sio:SIO_000628
miriam-gene:1103
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_provenance
{
dgn-np:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_assertion
dcterms:description
"[A G-to-A polymorphism detected in the first coding exon of the ChAT sequence may result in attenuated translation efficiency of ChAT mRNA and confer an increased risk for deterioration of memory and cognition functions in Alzheimer's disease.]. 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:12401548
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP110501.RAYHOfYRysy9XD-kS_-kkqp2zgZBml-PiceKwP1NcwcQs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:56+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" .
}