@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U
> .
@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:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_head
{
this:
np:hasAssertion
dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_assertion
;
np:hasProvenance
dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_provenance
;
np:hasPublicationInfo
dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_assertion
a
np:Assertion
.
dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_provenance
a
np:Provenance
.
dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGNc8b2e511b92aa3802fd2e43c514b97a8
sio:SIO_000628
miriam-gene:4137
,
lld:C0497327
;
a
sio:SIO_001121
.
}
dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_provenance
{
dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_assertion
dcterms:description
"[To determine whether functional connectivity is altered in subjects with mutations in the microtubule associated protein tau (MAPT) gene who were asymptomatic but were destined to develop dementia, and to compare these findings to those in subjects with behavioral variant frontotemporal dementia (bvFTD).]. 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:21849646
;
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:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:41+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" .
}