@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak
> .
@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:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_head
{
this:
np:hasAssertion
dgn-np:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_assertion
;
np:hasProvenance
dgn-np:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_provenance
;
np:hasPublicationInfo
dgn-np:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_assertion
a
np:Assertion
.
dgn-np:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_provenance
a
np:Provenance
.
dgn-np:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_assertion
{
miriam-gene:3265
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGNb2c4dc916ca5a5c6f5905427bc9f13b7
sio:SIO_000628
miriam-gene:3265
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_provenance
{
dgn-np:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_assertion
dcterms:description
"[These `giant` spindles were not associated with any evidence of structural damage of the cortex or the thalami and should be considered as phenotypic feature of sleep EEG activity in Costello syndrome because of HRAS mutation.]. 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:21633259
;
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:NP618082.RA6C7LZCE-I0_sikYt91DCu5vjdb5-dX57yNplYe6r_Ak130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}