@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A
> .
@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:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_head
{
this:
np:hasAssertion
dgn-np:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_assertion
;
np:hasProvenance
dgn-np:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_provenance
;
np:hasPublicationInfo
dgn-np:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_assertion
a
np:Assertion
.
dgn-np:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_provenance
a
np:Provenance
.
dgn-np:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_assertion
{
miriam-gene:793
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN9284cb1225c0165f8d9ad9a41b93975f
sio:SIO_000628
miriam-gene:793
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_provenance
{
dgn-np:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_assertion
dcterms:description
"[Comparison of diseased human brain tissue with age- and sex-matched controls yielded significant decreases (60-88%) in calbindin protein and mRNA in the substantia nigra (Parkinson disease), in the corpus striatum (Huntington disease), in the nucleus basalis (Alzheimer disease), and in the hippocampus and nucleus raphe dorsalis (Parkinson, Huntington, and Alzheimer diseases) but not in the cerebellum, neocortex, amygdala, or locus ceruleus.]. 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:2140897
;
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:NP830742.RABJsKrl78IGHyEiY5_HPKTneXNrYaaCJmUmPs3o9_-3A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}