@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP437905.RAkeDxft_q2l6UWgAwoUuhxODlMyVeuDDWW9soLCbQQd4
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP437905.RAkeDxft_q2l6UWgAwoUuhxODlMyVeuDDWW9soLCbQQd4130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP437905.RAkeDxft_q2l6UWgAwoUuhxODlMyVeuDDWW9soLCbQQd4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP437905.RAkeDxft_q2l6UWgAwoUuhxODlMyVeuDDWW9soLCbQQd4130_assertion
a
np:Assertion
.
dgn-np:NP437905.RAkeDxft_q2l6UWgAwoUuhxODlMyVeuDDWW9soLCbQQd4130_provenance
a
np:Provenance
.
dgn-np:NP437905.RAkeDxft_q2l6UWgAwoUuhxODlMyVeuDDWW9soLCbQQd4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP437905.RAkeDxft_q2l6UWgAwoUuhxODlMyVeuDDWW9soLCbQQd4130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGNf8a16534484299ae63ded6dcfdd6cd63
sio:SIO_000628
miriam-gene:4137
,
lld:C0497327
;
a
sio:SIO_001121
.
}
dgn-np:NP437905.RAkeDxft_q2l6UWgAwoUuhxODlMyVeuDDWW9soLCbQQd4130_provenance
{
dgn-np:NP437905.RAkeDxft_q2l6UWgAwoUuhxODlMyVeuDDWW9soLCbQQd4130_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-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:NP437905.RAkeDxft_q2l6UWgAwoUuhxODlMyVeuDDWW9soLCbQQd4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:03+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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}