@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8
> .
@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:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_head
{
this:
np:hasAssertion
dgn-np:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_assertion
;
np:hasProvenance
dgn-np:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_provenance
;
np:hasPublicationInfo
dgn-np:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_assertion
a
np:Assertion
.
dgn-np:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_provenance
a
np:Provenance
.
dgn-np:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_assertion
{
miriam-gene:1103
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGN9afa41e55ed3fad6a7585bfbf32b04a5
sio:SIO_000628
miriam-gene:1103
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_provenance
{
dgn-np:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_assertion
dcterms:description
"[The subnormal choline acetyltransferase (ChoAcTase) activity in the cerebral cortex of patients with Alzheimer disease (AD) is thought to originate from the loss of cholinergic neurons in the nucleus basalis of Meynert (nbM).]. 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:1409664
;
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:NP594979.RA1pe2vcqf1tCc51PPV7qnsca42AZedptMvY40FusvlE8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:57+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" .
}