@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU
> .
@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 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:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_head
{
this:
np:hasAssertion
dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_assertion
;
np:hasProvenance
dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_provenance
;
np:hasPublicationInfo
dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_assertion
a
np:Assertion
.
dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_provenance
a
np:Provenance
.
dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C1389280
a
ncit:C7057
.
dgn-gda:DGNbb87b96a6688f424154f469d176d262a
sio:SIO_000628
miriam-gene:3918
,
lld:C1389280
;
a
sio:SIO_001121
.
}
dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_provenance
{
dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_assertion
dc:description
"[The authors report the ninth case of progressive familial encephalopathy in infancy, with calcification of the basal ganglia and chronic cerebrospinal fluid (CSF) lymphocytosis, as recently described by Aicardi and Goutieres.]. 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:3731164
;
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:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_publicationInfo
{
this:
dc:created
"2014-10-02T12:40:16+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}