@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c
> .
@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/
> .
dgn-np:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_head
{
this:
np:hasAssertion
dgn-np:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_assertion
;
np:hasProvenance
dgn-np:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_provenance
;
np:hasPublicationInfo
dgn-np:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_assertion
a
np:Assertion
.
dgn-np:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_provenance
a
np:Provenance
.
dgn-np:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0038868
a
ncit:C7057
.
dgn-gda:DGNd20eecf340b630153224fcbca3c0b89d
sio:SIO_000628
miriam-gene:4137
,
lld:C0038868
;
a
sio:SIO_001121
.
}
dgn-np:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_provenance
{
dgn-np:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_assertion
dcterms:description
"[Recent studies have shown an association between an extended tau haplotype (H1) that covers the entire human tau gene and progressive supranuclear palsy or, more inconsistently, other neurodegenerative disorders, such as corticobasal degeneration, Parkinson disease, Alzheimer disease, and frontotemporal dementia (FTD).]. 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:12056929
;
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:NP357333.RASmL-LEzlDylkG4Krtrh1VfZkawtCiJ_QWJ3hFECZm3c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:27+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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}