@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o
> .
@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/v3.0.0/void/
> .
dgn-np:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_head
{
this:
np:hasAssertion
dgn-np:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_assertion
;
np:hasProvenance
dgn-np:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_provenance
;
np:hasPublicationInfo
dgn-np:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_assertion
a
np:Assertion
.
dgn-np:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_provenance
a
np:Provenance
.
dgn-np:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0338451
a
ncit:C7057
.
dgn-gda:DGNe361123f7144ae3191ca730299cade35
sio:SIO_000628
miriam-gene:4137
,
lld:C0338451
;
a
sio:SIO_001121
.
}
dgn-np:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_provenance
{
dgn-np:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_assertion
dcterms:description
"[However, the existence of tauopathies that are devoid of Aβ deposits, together with the discovery of mutations in the tau gene leading to frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17T), confirmed the importance of tau per se in disease.]. 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:24050961
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP546152.RA4xUOVSMIsuzFupoq6NXZiL3Zf-NK5pXMye_ah49kX3o130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:03+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}