@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c
> .
@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:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_head
{
this:
np:hasAssertion
dgn-np:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_assertion
;
np:hasProvenance
dgn-np:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_provenance
;
np:hasPublicationInfo
dgn-np:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_assertion
a
np:Assertion
.
dgn-np:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_provenance
a
np:Provenance
.
dgn-np:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_assertion
{
miriam-gene:1201
a
ncit:C16612
.
lld:C0027877
a
ncit:C7057
.
dgn-gda:DGN24651862a7fc948eb1764ebed3aec614
sio:SIO_000628
miriam-gene:1201
,
lld:C0027877
;
a
sio:SIO_001121
.
}
dgn-np:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_provenance
{
dgn-np:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_assertion
dcterms:description
"[The juvenile form of neuronal ceroid lipofuscinoses (JNCLs), or Batten disease, results from mutations in the CLN3 gene, and it is characterized by the accumulation of lipopigments in the lysosomes of several cell types and by extensive neuronal death.]. 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:17475770
;
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:NP367615.RA1iTnfbCm_mnZTdtIFlxefJoQtRY2k2F1QZcqfsVKE9c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:35+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" .
}