@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A
> .
@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:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_head
{
this:
np:hasAssertion
dgn-np:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_assertion
;
np:hasProvenance
dgn-np:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_provenance
;
np:hasPublicationInfo
dgn-np:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_assertion
a
np:Assertion
.
dgn-np:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_provenance
a
np:Provenance
.
dgn-np:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0949664
a
ncit:C7057
.
dgn-gda:DGN6606e1e7696efa3f661188c7680cb7f6
sio:SIO_000628
miriam-gene:4137
,
lld:C0949664
;
a
sio:SIO_001121
.
}
dgn-np:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_provenance
{
dgn-np:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_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-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:NP518881.RAIWc5p8uTPViF8HGMPJm-d0p5_ySrGi_qxSqyBIHmy-A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:40+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" .
}