@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM
> .
@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:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_head
{
this:
np:hasAssertion
dgn-np:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_assertion
;
np:hasProvenance
dgn-np:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_provenance
;
np:hasPublicationInfo
dgn-np:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_assertion
a
np:Assertion
.
dgn-np:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_provenance
a
np:Provenance
.
dgn-np:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_assertion
{
miriam-gene:4538
a
ncit:C16612
.
lld:C0917796
a
ncit:C7057
.
dgn-gda:DGN102fa5048c6db941adaabf951b7c4a24
sio:SIO_000628
miriam-gene:4538
,
lld:C0917796
;
a
sio:SIO_001121
.
}
dgn-np:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_provenance
{
dgn-np:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_assertion
dcterms:description
"[Three pathogenic mutations (positions 11778/ND4, 3460/ND1 and 14484/ND6) account for the majority of LHON cases and they affect genes that encode for different subunits of mitochondrial complex I. Excitotoxic injury to retinal ganglion cells and the optic nerve has been previously hypothesized, especially given the high susceptibility of this neural cell type to glutamate toxicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:15342361
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP23870.RAnwZpz6j8XA0PzKGm_sGYnetNMt66s5Jlu9XCKz5iKuM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:09+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" .
}