@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU130_assertion
;
np:hasProvenance
dgn-np:NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU130_provenance
;
np:hasPublicationInfo
dgn-np:NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU130_assertion
a
np:Assertion
.
dgn-np:NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU130_provenance
a
np:Provenance
.
dgn-np:NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0338451
a
ncit:C7057
.
dgn-gda:DGN8c24c1831be49458ed04855712496678
sio:SIO_000628
miriam-gene:4137
,
lld:C0338451
;
a
sio:SIO_001121
.
}
dgn-np:NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU130_provenance
{
dgn-np:NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU130_assertion
dcterms:description
"[The analysis of tau gene and the study of familial cases of tauopathies have led to the discovery of tau gene mutations that cause inherited dementia designated as Frontotemporal dementia (FTD) with parkinsonism linked to chromosome 17 (FTDP-17).]. 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:15056452
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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 .
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dgn-np:NP199340.RAGxwx--8Hja9GuGwQeU2FT6xgujhLHY32Qt2q9LgrEjU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}