@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY
> .
@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:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_head
{
this:
np:hasAssertion
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_assertion
;
np:hasProvenance
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_provenance
;
np:hasPublicationInfo
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_assertion
a
np:Assertion
.
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_provenance
a
np:Provenance
.
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_assertion
{
miriam-gene:404672
a
ncit:C16612
.
lld:C0231341
a
ncit:C7057
.
dgn-gda:DGN182cd11726260599f2ee149a92bd799e
sio:SIO_000628
miriam-gene:404672
,
lld:C0231341
;
a
sio:SIO_001121
.
}
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_provenance
{
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_assertion
dcterms:description
"[Studies presented at the workshop described important new insights into the phenotypic complexity of XP, CS and TTD, renewed focus on the neurological manifestations of each of these diseases, as well as keen interest in the role of oxidative stress and mitochondrial dysfunction in neurodegenerative processes and normal and/or premature aging.]. 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:17361460
;
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:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}