@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_head
{
this:
np:hasAssertion
dgn-np:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_assertion
;
np:hasProvenance
dgn-np:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_provenance
;
np:hasPublicationInfo
dgn-np:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_assertion
a
np:Assertion
.
dgn-np:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_provenance
a
np:Provenance
.
dgn-np:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0242422
a
ncit:C7057
.
dgn-gda:DGNf1fd116e291b42f9aaff522cc4d08fda
sio:SIO_000628
miriam-gene:4137
,
lld:C0242422
;
a
sio:SIO_001121
.
}
dgn-np:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_provenance
{
dgn-np:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_assertion
dcterms:description
"[Extensive neuronal loss and aggregation of tau as cytoplasmic inclusions in neurons and glial cells in selected cortical and subcortical regions is the most striking characteristic of frontotemporal dementia and parkinsonism linked to chromosome 17, which is caused by exonic or intronic mutations in the tau gene.]. 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:10362789
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP254522.RAGXK1W4JlbRSV5crrTPvxpdhM3x2RJ_TCZHz18A6JdXA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:41+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}