@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU
> .
@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:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_head
{
this:
np:hasAssertion
dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_assertion
;
np:hasProvenance
dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_provenance
;
np:hasPublicationInfo
dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_assertion
a
np:Assertion
.
dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_provenance
a
np:Provenance
.
dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_assertion
{
miriam-gene:1201
a
ncit:C16612
.
lld:C0085078
a
ncit:C7057
.
dgn-gda:DGN5b89409239463d26a8075e97e329df9c
sio:SIO_000628
miriam-gene:1201
,
lld:C0085078
;
a
sio:SIO_001121
.
}
dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_provenance
{
dgn-np:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_assertion
dcterms:description
"[To use the Unified Batten Disease Rating Scale (UBDRS) to measure the rate of decline in physical and functional capability domains in patients with juvenile neuronal ceroid lipofuscinosis (JNCL) or Batten disease, a neurodegenerative lysosomal storage disorder.]. 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:22013180
;
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:NP515758.RANi6Pm84IPMUHlLOwdL25_eaSknea7Hi21UrXeyDuoHU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:07+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" .
}