@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w
> .
@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:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_head
{
this:
np:hasAssertion
dgn-np:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_assertion
;
np:hasProvenance
dgn-np:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_provenance
;
np:hasPublicationInfo
dgn-np:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_assertion
a
np:Assertion
.
dgn-np:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_provenance
a
np:Provenance
.
dgn-np:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_assertion
{
miriam-gene:6442
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGNc769fe5430b92ad0029812ef0a84f1c1
sio:SIO_000628
miriam-gene:6442
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_provenance
{
dgn-np:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_assertion
dcterms:description
"[The loss of neurons and synaptic connections is selective and causes deficiencies in cholinergic and other neurotransmitter systems, leading to cognitive dysfunction, psychiatric and behavioral disturbances, and eventual loss of ability to perform ADL.]. 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:9809105
;
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:NP711718.RAv7PZiwHwbTi3xnXNSRXEeiTXOuR5Ww1XG5fW3O2wc6w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:12+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" .
}