@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg
> .
@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:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_head
{
this:
np:hasAssertion
dgn-np:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_assertion
;
np:hasProvenance
dgn-np:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_provenance
;
np:hasPublicationInfo
dgn-np:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_assertion
a
np:Assertion
.
dgn-np:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_provenance
a
np:Provenance
.
dgn-np:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_assertion
{
miriam-gene:1103
a
ncit:C16612
.
lld:C0494463
a
ncit:C7057
.
dgn-gda:DGN495d5d83addfc868129ed81c2136b32e
sio:SIO_000628
miriam-gene:1103
,
lld:C0494463
;
a
sio:SIO_001121
.
}
dgn-np:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_provenance
{
dgn-np:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_assertion
dcterms:description
"[The genes encoding choline acetyltransferase (ChAT) and its vesicular transporter (VAChT), CHAT and SLC18A3 respectively, map to the linked region of chromosome 10 and are therefore both positional and obvious functional candidate genes for late-onset AD.]. 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:12759818
;
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:NP827867.RA4aAElnRxJhLZOLSp4eyH767fsMPIWR9Jbgc4g1fJCHg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:26+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" .
}