@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY
> .
@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:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_head
{
this:
np:hasAssertion
dgn-np:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_assertion
;
np:hasProvenance
dgn-np:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_provenance
;
np:hasPublicationInfo
dgn-np:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_assertion
a
np:Assertion
.
dgn-np:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_provenance
a
np:Provenance
.
dgn-np:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_assertion
{
miriam-gene:4566
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN22bae47ff086108c23a9f7989d88e3f9
sio:SIO_000628
miriam-gene:4566
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_provenance
{
dgn-np:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_assertion
dcterms:description
"[Point mutations of mitochondrial DNA have been described in the muscle of patients with syndromes of myoclonic epilepsy and ragged red fibres (MERRF) and of mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS).]. 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:1674297
;
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:NP504324.RA94VML2o1lwiIsCjPUj5EPl2EaSiQOKAmlWnAo22FQjY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}