@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg
> .
@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:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_head
{
this:
np:hasAssertion
dgn-np:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_assertion
;
np:hasProvenance
dgn-np:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_provenance
;
np:hasPublicationInfo
dgn-np:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_assertion
a
np:Assertion
.
dgn-np:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_provenance
a
np:Provenance
.
dgn-np:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0236642
a
ncit:C7057
.
dgn-gda:DGNe9a57e80ad4c2f87a5fd85796a75e115
sio:SIO_000628
miriam-gene:4137
,
lld:C0236642
;
a
sio:SIO_001121
.
}
dgn-np:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_provenance
{
dgn-np:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_assertion
dcterms:description
"[The recent discovery of tau gene mutations in FTD with Parkinsonism linked to chromosome 17 has reinforced the direct role attributed to abnormal tau proteins (hyperphosphorylation) and thus raised the possibility to target specifically these processes by drugs (aetiopathogenic compounds).]. 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:12672175
;
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:NP389421.RAy7KUf7vKi1QkJ8mcNGMhHsgaec8BmHiHbnoglO4tPGg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:41+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" .
}