@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ
> .
@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:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_head
{
this:
np:hasAssertion
dgn-np:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_assertion
;
np:hasProvenance
dgn-np:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_assertion
a
np:Assertion
.
dgn-np:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_provenance
a
np:Provenance
.
dgn-np:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_assertion
{
miriam-gene:7321
a
ncit:C16612
.
lld:C0432072
a
ncit:C7057
.
dgn-gda:DGNa7d319515aaeb82556ef6a09dcdae58b
sio:SIO_000628
miriam-gene:7321
,
lld:C0432072
;
a
sio:SIO_001121
.
}
dgn-np:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_provenance
{
dgn-np:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_assertion
dcterms:description
"[In these patients, the electroclinical pattern of theta waves (probably unrelated to epilepsy) and the SW and SFT, even with mild mental retardation (MR) or no MR and without dysmorphic features, suggest that the r(20) syndrome may be present.]. 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:9738673
;
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:NP715182.RAw_UdAHF14E0l8W_Coh1-5a3ISVBUaGOhWTqnW3yRPpQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:14+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" .
}