@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg
> .
@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:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_head
{
this:
np:hasAssertion
dgn-np:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_assertion
;
np:hasProvenance
dgn-np:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_provenance
;
np:hasPublicationInfo
dgn-np:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_assertion
a
np:Assertion
.
dgn-np:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_provenance
a
np:Provenance
.
dgn-np:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGNf3c379a10c61b8d30fcbb354b05eaaa9
sio:SIO_000628
miriam-gene:4137
,
lld:C0085400
;
a
sio:SIO_001121
.
}
dgn-np:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_provenance
{
dgn-np:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_assertion
dcterms:description
"[Tau pathology, in the form of neurofibrillary tangles (NFTs) and glial cell tangles, was present in six cases of FTD with parkinsonism linked to chromosome 17, five of these cases resulting from +16 splice-site mutation and one from +13 mutation 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:14720172
;
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:NP427873.RAS9EP-H9g1vLbR9lagfYlOFZFeJHcvpBARFpZd7GKrPg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:59+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" .
}