@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA
> .
@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:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_head
{
this:
np:hasAssertion
dgn-np:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_assertion
;
np:hasProvenance
dgn-np:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_provenance
;
np:hasPublicationInfo
dgn-np:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_assertion
a
np:Assertion
.
dgn-np:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_provenance
a
np:Provenance
.
dgn-np:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_assertion
{
miriam-gene:2937
a
ncit:C16612
.
lld:C0037019
a
ncit:C7057
.
dgn-gda:DGNf35d8b84ec2bd22dfeea48deb022841d
sio:SIO_000628
miriam-gene:2937
,
lld:C0037019
;
a
sio:SIO_001121
.
}
dgn-np:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_provenance
{
dgn-np:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_assertion
dcterms:description
"[These findings conflict with those in multiple system atrophy and other prion diseases such as fatal familial insomnia, which enter the differential diagnosis of GSS and are characterized by prominently disrupted sleep-wake and BcT degrees cycles.]. 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:18550428
;
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:NP724554.RAz4UMu6R-Zt-aI_spYPp2cyIwxsyObGqXCi-gFjDcGfA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}