@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE
> .
@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:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_head
{
this:
np:hasAssertion
dgn-np:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_assertion
;
np:hasProvenance
dgn-np:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_provenance
;
np:hasPublicationInfo
dgn-np:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_assertion
a
np:Assertion
.
dgn-np:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_provenance
a
np:Provenance
.
dgn-np:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_assertion
{
miriam-gene:5443
a
ncit:C16612
.
lld:C0037769
a
ncit:C7057
.
dgn-gda:DGNf8e2cd1ccedfb8ae67ae8d4384b4d0e9
sio:SIO_000628
miriam-gene:5443
,
lld:C0037769
;
a
sio:SIO_001121
.
}
dgn-np:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_provenance
{
dgn-np:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_assertion
dcterms:description
"[Given the very poor prognosis of infantile spasms especially in such conditions as cerebral palsy, the combination of ACTH and vigabatrin appears to be an interesting therapy advance with very few side effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:8980841
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP26706.RA4tmo0FzEeERGZt-5HJHRX4AxVHUeXKVf6ToJBuYT4FE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:11+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" .
}