@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI
> .
@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:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_head
{
this:
np:hasAssertion
dgn-np:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_assertion
;
np:hasProvenance
dgn-np:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_provenance
;
np:hasPublicationInfo
dgn-np:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_assertion
a
np:Assertion
.
dgn-np:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_provenance
a
np:Provenance
.
dgn-np:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_assertion
{
miriam-gene:2131
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNe435a1b4433f79d176a0a2ffe60601a6
sio:SIO_000628
miriam-gene:2131
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_provenance
{
dgn-np:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_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:NP394882.RA-dhdje-vHE3jMBH5QBvaEYt3jUvxd5YHZZr1SMka0cI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}