@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM
> .
@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:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_head
{
this:
np:hasAssertion
dgn-np:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_assertion
;
np:hasProvenance
dgn-np:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_provenance
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np:hasPublicationInfo
dgn-np:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_assertion
a
np:Assertion
.
dgn-np:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_provenance
a
np:Provenance
.
dgn-np:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0751072
a
ncit:C7057
.
dgn-gda:DGN15c951913eb4514c3eb4fa173f7953cd
sio:SIO_000628
miriam-gene:4137
,
lld:C0751072
;
a
sio:SIO_001121
.
}
dgn-np:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_provenance
{
dgn-np:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_assertion
dcterms:description
"[We compared tau pathology in different astrocyte phenotypes and oligodendroglial inclusions with that in neurons in a large series of tauopathies, including progressive supranuclear palsy, corticobasal degeneration, argyrophilic grain disease, Pick disease, frontotemporal lobar degenerations (FTLD) associated with mutations in the tau gene, globular glial tauopathy (GGT), and tauopathy in the elderly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:24335532
;
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:NP546262.RAdl8fnb8A0ayd0X3ZJgmdeJ6LAfvOR1VkA22NjQ1K4FM130_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
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;
pav:authoredBy
<
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> , <
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
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pav:version
"v3.0.0" .
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