@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII
> .
@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:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_head
{
this:
np:hasAssertion
dgn-np:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_assertion
;
np:hasProvenance
dgn-np:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_provenance
;
np:hasPublicationInfo
dgn-np:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_assertion
a
np:Assertion
.
dgn-np:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_provenance
a
np:Provenance
.
dgn-np:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0338451
a
ncit:C7057
.
dgn-gda:DGN7c3ebac28b6eb196568a7d56bb1e825a
sio:SIO_000628
miriam-gene:4137
,
lld:C0338451
;
a
sio:SIO_001121
.
}
dgn-np:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_provenance
{
dgn-np:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_assertion
dcterms:description
"[Mutations in the microtubule-associated protein tau gene (MAPT) can cause frontotemporal dementia with Parkinsonism linked to the chromosome 17, and are associated with the risk for progressive supranuclear palsy, Parkinson's disease, corticobasal degeneration, and multiple system atrophy.]. 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:23001634
;
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:NP546146.RAbApovLfnNhkkcqVbAQPzd7oNVm8sa2W-7CQefX1MFII130_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" .
}