@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM
> .
@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:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_head
{
this:
np:hasAssertion
dgn-np:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_assertion
;
np:hasProvenance
dgn-np:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_provenance
;
np:hasPublicationInfo
dgn-np:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_assertion
a
np:Assertion
.
dgn-np:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_provenance
a
np:Provenance
.
dgn-np:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_assertion
{
miriam-gene:28954
a
ncit:C16612
.
lld:C0027404
a
ncit:C7057
.
dgn-gda:DGN8a16874498a7995f69f402add49a651e
sio:SIO_000628
miriam-gene:28954
,
lld:C0027404
;
a
sio:SIO_001121
.
}
dgn-np:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_provenance
{
dgn-np:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_assertion
dcterms:description
"[Males with multiple SOREMPs compared with those with no SOREMPs had shorter rapid eye movement (REM) latency during NPSG, were sleepier on the MSLT and reported increased sleepiness, hypnagogic hallucinations and cataplexy-like symptoms, suggesting a narcolepsy-like phenotype.]. 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:16597649
;
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:NP454621.RAkOguNVu3YOVKcxkrkHNbOjJbWa2sO_7xu_1_pnZUsYM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:31+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" .
}