@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0
> .
@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:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_head
{
this:
np:hasAssertion
dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_assertion
;
np:hasProvenance
dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_assertion
a
np:Assertion
.
dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_provenance
a
np:Provenance
.
dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0009207
a
ncit:C7057
.
dgn-gda:DGN967592696bd321ec6729aa756391715b
sio:SIO_000628
miriam-gene:5621
,
lld:C0009207
;
a
sio:SIO_001121
.
}
dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_provenance
{
dgn-np:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_assertion
dcterms:description
"[Our clinical and neurophysiological study seems to indicate that a particular condition of severe sleep disruption, similar to some extent to that reported in the fatal familial insomnia and in the Morvan fibrillary chorea, which has been indicated as Agrypnia Excitata in recent literature, might be associated with the Mulvihill-Smith syndrome.]. 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:16364148
;
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:NP315652.RArPet0fCQ9qf1IsP4uHGO7k5Lytx9dbZ8UvYCrJyYdZ0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}