@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs
> .
@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#
> .
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_head
{
this:
np:hasAssertion
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_assertion
;
np:hasProvenance
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_provenance
;
np:hasPublicationInfo
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_assertion
a
np:Assertion
.
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_provenance
a
np:Provenance
.
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0393570
a
ncit:C7057
.
dgn-gda:DGN9b7942471106a9e93168c62be47c24f7
sio:SIO_000628
miriam-gene:4137
,
lld:C0393570
;
a
sio:SIO_001121
.
}
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_provenance
{
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_assertion
dcterms:description
"[The presence of microtubule-associated-protein-tau-based pathological features in some patients and the discovery, in some familial cases, of mutations in the tau gene links FTD to other forms of tauopathy, such as progressive supranuclear palsy and corticobasal degeneration.]. 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:16239184
;
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 .
}
dgn-np:NP326243.RAEKrUG9QHtl4iDJ1W92eaHldYqXKjsCz8E_UV1p6YJGs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}