@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY
> .
@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:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_assertion
;
np:hasProvenance
dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_provenance
;
np:hasPublicationInfo
dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_assertion
a
np:Assertion
.
dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_provenance
a
np:Provenance
.
dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:2395
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNad90ed0b7312048c9749e80549572c30
sio:SIO_000628
miriam-gene:2395
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_provenance
{
dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_assertion
dcterms:description
"[The role of genetic background is discussed on the light of the oxidative stress implication, focusing on both complex neurodegenerative diseases (Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis) and monogenic neurological disorders (Huntington's disease, Ataxia telangiectasia, Friedreich Ataxia and others).]. 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:18952194
;
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:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:08+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" .
}