@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs
> .
@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:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_head
{
this:
np:hasAssertion
dgn-np:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_assertion
;
np:hasProvenance
dgn-np:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_provenance
;
np:hasPublicationInfo
dgn-np:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_assertion
a
np:Assertion
.
dgn-np:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_provenance
a
np:Provenance
.
dgn-np:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_assertion
{
miriam-gene:10971
a
ncit:C16612
.
lld:C0038868
a
ncit:C7057
.
dgn-gda:DGN67c4c13262a598dbaca4adc796c988b0
sio:SIO_000628
miriam-gene:10971
,
lld:C0038868
;
a
sio:SIO_001121
.
}
dgn-np:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_provenance
{
dgn-np:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_assertion
dcterms:description
"[Recent studies have reported high familial aggregation in PSP patients, and it has been widely demonstrated that Microtuble Associated Protein Tau (MAPT) gene mutations are causative of monogenic autosomal dominant PSP.]. 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:21568901
;
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:NP555669.RABEGs8rJGO5VnAHIrtjfyEvax3R5azN3I2rDSwk3NTYs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:35+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" .
}