@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE
> .
@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:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_head
{
this:
np:hasAssertion
dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_assertion
;
np:hasProvenance
dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_provenance
;
np:hasPublicationInfo
dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_assertion
a
np:Assertion
.
dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_provenance
a
np:Provenance
.
dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_assertion
{
miriam-gene:43
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGN99b3e04f4948340404b47924057fcbb6
sio:SIO_000628
miriam-gene:43
,
lld:C0524851
;
a
sio:SIO_001122
.
}
dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_provenance
{
dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_assertion
dcterms:description
"[Variant-specific causal involvement of AChE in the progression of both neurodegenerative diseases and neuromuscular syndromes raises the possibility that future therapeutic drugs might target specific AChE variant (s) or the corresponding RNA transcripts.]. 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:16516310
;
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:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:11+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" .
}