@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg
> .
@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:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_head
{
this:
np:hasAssertion
dgn-np:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_assertion
;
np:hasProvenance
dgn-np:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_provenance
;
np:hasPublicationInfo
dgn-np:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_assertion
a
np:Assertion
.
dgn-np:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_provenance
a
np:Provenance
.
dgn-np:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0338451
a
ncit:C7057
.
dgn-gda:DGNb5bbc55079c403b31f09fae29f298ea6
sio:SIO_000628
miriam-gene:4137
,
lld:C0338451
;
a
sio:SIO_001121
.
}
dgn-np:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_provenance
{
dgn-np:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_assertion
dcterms:description
"[However, since 1998, the identification of more than 25 mutations in the tau gene, associated with frontotemporal dementia and parkinsonism linked to chromosome 17, has demonstrated that tau dysfunction can lead to neurodegeneration and the development of clinical symptoms.]. 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:12470988
;
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:NP376894.RAJ6My4UfOt-8dS6CtF9zoLtbg0PlactQKxox6ek8gwyg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:36+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" .
}