@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o
> .
@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:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_head
{
this:
np:hasAssertion
dgn-np:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_assertion
;
np:hasProvenance
dgn-np:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_provenance
;
np:hasPublicationInfo
dgn-np:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_assertion
a
np:Assertion
.
dgn-np:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_provenance
a
np:Provenance
.
dgn-np:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_assertion
{
miriam-gene:653590
a
ncit:C16612
.
lld:C0751651
a
ncit:C7057
.
dgn-gda:DGN3ffd84babfc4946d45e35835c6adb96c
sio:SIO_000628
miriam-gene:653590
,
lld:C0751651
;
a
sio:SIO_001121
.
}
dgn-np:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_provenance
{
dgn-np:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_assertion
dcterms:description
"[Our findings that the frequency of the haplotype AAC, and AAT were significantly higher in the unaffected cases and the frequencies of haplotype GGT were significantly higher in LHON cases, indicate that it might have a role in the penetrance of this mitochondrial disease.]. 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:23973714
;
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:NP878884.RACNa2mI8Y5JjrFgiL2GD_sjDacXUSgZeNx34Rk-oJf0o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}