@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU
> .
@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:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_head
{
this:
np:hasAssertion
dgn-np:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_assertion
;
np:hasProvenance
dgn-np:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_provenance
;
np:hasPublicationInfo
dgn-np:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_assertion
a
np:Assertion
.
dgn-np:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_provenance
a
np:Provenance
.
dgn-np:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_assertion
{
miriam-gene:51557
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNddf2c218fab47637626991b2c664c0fb
sio:SIO_000628
miriam-gene:51557
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_provenance
{
dgn-np:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_assertion
dcterms:description
"[Although antecedent neurological conditions have preceded LGS in some patients, others with similar ills fail to develop this syndrome, and precise charting of the pathway between any presumed aetiology and the epilepsy has eluded researchers.]. 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:11844713
;
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:NP867620.RAe1jtZ5Wb9qzAvtrR-5CPZ5WkH8kf3Ph293pLZYkKgBU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:50+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" .
}