@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_assertion
;
np:hasProvenance
dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_provenance
;
np:hasPublicationInfo
dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_assertion
a
np:Assertion
.
dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_provenance
a
np:Provenance
.
dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_assertion
{
miriam-gene:7376
a
ncit:C16612
.
lld:C0678236
a
ncit:C7057
.
dgn-gda:DGN50e0206cf5629f40a80a9456b9dcaf58
sio:SIO_000628
miriam-gene:7376
,
lld:C0678236
;
a
sio:SIO_001121
.
}
dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_provenance
{
dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_assertion
dcterms:description
"[Topics discussed included the natural history and clinical features of the diseases, clinical and laboratory diagnosis of these rare diseases, therapeutic strategies, mouse models of neurodegeneration, molecular analysis of accelerated aging, impact of transcriptional defects and mitochondrial dysfunction on neurodegeneration, and biochemical insights into mechanisms of NER and base excision repair.]. 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:21708183
;
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:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:42+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" .
}