@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc
> .
@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:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_head
{
this:
np:hasAssertion
dgn-np:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_assertion
;
np:hasProvenance
dgn-np:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_provenance
;
np:hasPublicationInfo
dgn-np:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_assertion
a
np:Assertion
.
dgn-np:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_provenance
a
np:Provenance
.
dgn-np:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0338451
a
ncit:C7057
.
dgn-gda:DGNbc1909f4330e20c1a4806eb9f7fa8aa3
sio:SIO_000628
miriam-gene:4137
,
lld:C0338451
;
a
sio:SIO_001121
.
}
dgn-np:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_provenance
{
dgn-np:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_assertion
dcterms:description
"[Hereditary frontotemporal dementia (FTD) is an autosomal dominant neurodegenerative disorder that is associated with mutations in the tau gene and with the pathological accumulation of hyperphosphorylated tau protein in affected brain cells in about a quarter of cases.]. 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:11571213
;
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:NP331003.RANh-tgEVIsr-ltkOUK-MM28FpbK9m9Yn7hTee93fFMKc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:15+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" .
}