@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU
> .
@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:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_head
{
this:
np:hasAssertion
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_assertion
;
np:hasProvenance
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_provenance
;
np:hasPublicationInfo
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_assertion
a
np:Assertion
.
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_provenance
a
np:Provenance
.
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN505722fdd97601ef5c1a4d7dc0e59308
sio:SIO_000628
miriam-gene:1437
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_provenance
{
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_assertion
dcterms:description
"[Both AChE-R and AChE-S splice variants as well as several heavier AChE complexes were detected in brain homogenates from the parietal cortex of patients with or without Alzheimer's disease (AD) as well as the cerebrospinal fluid (CSF) of AD patients, compatible with the assumption that CSF AChEs might originate from CNS neurons.]. 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:15009666
;
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:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:33+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" .
}