@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4
> .
@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:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_head
{
this:
np:hasAssertion
dgn-np:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_assertion
;
np:hasProvenance
dgn-np:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_provenance
;
np:hasPublicationInfo
dgn-np:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_assertion
a
np:Assertion
.
dgn-np:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_provenance
a
np:Provenance
.
dgn-np:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C1389280
a
ncit:C7057
.
dgn-gda:DGNd0571b435b7b6eb125f3f0e53051071e
sio:SIO_000628
miriam-gene:1437
,
lld:C1389280
;
a
sio:SIO_001121
.
}
dgn-np:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_provenance
{
dgn-np:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_assertion
dcterms: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:NP674014.RAQSpKb7hJDg74Jk5fGcI9WC2YrptpY5JkoX5wFd4-7l4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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" .
}