@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck
> .
@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:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_head
{
this:
np:hasAssertion
dgn-np:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_assertion
;
np:hasProvenance
dgn-np:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_provenance
;
np:hasPublicationInfo
dgn-np:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_assertion
a
np:Assertion
.
dgn-np:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_provenance
a
np:Provenance
.
dgn-np:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_assertion
{
miriam-gene:9211
a
ncit:C16612
.
lld:C0011581
a
ncit:C7057
.
dgn-gda:DGN7c17822d5da436f8c5635f908966950c
sio:SIO_000628
miriam-gene:9211
,
lld:C0011581
;
a
sio:SIO_001121
.
}
dgn-np:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_provenance
{
dgn-np:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_assertion
dcterms:description
"[A standardized depression screen was administered to 94 individuals from 11 families with mutations in LGI1, including 38 mutation carriers with epilepsy (AC), 11 clinically unaffected mutation carriers (UC), and 45 noncarriers (NC).]. 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:20659151
;
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:NP279449.RAqLPhaSclN4yvtu0SIdtPx-QD3XcwFq_yyq48v6W1Bck130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}