@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8
> .
@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:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_head
{
this:
np:hasAssertion
dgn-np:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_assertion
;
np:hasProvenance
dgn-np:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_provenance
;
np:hasPublicationInfo
dgn-np:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_assertion
a
np:Assertion
.
dgn-np:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_provenance
a
np:Provenance
.
dgn-np:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0162534
a
ncit:C7057
.
dgn-gda:DGN9f06a8f5205c3a26557d90276c3fc87e
sio:SIO_000628
miriam-gene:5621
,
lld:C0162534
;
a
sio:SIO_001121
.
}
dgn-np:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_provenance
{
dgn-np:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_assertion
dcterms:description
"[Fatal familial insomnia (FFI) is an inherited prion disease characterized by progressive insomnia and dysautonomia with only modest cognitive impairment early in the disease, associated with atrophy and gliosis in the medial thalamus, but without spongiform change.]. 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:9270595
;
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:NP1379392.RAjaDDDzR4pwRArvJM_MGZc7UHgnWSGYnHxU6Fv3Pz_J8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:11+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" .
}