@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ
> .
@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:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_head
{
this:
np:hasAssertion
dgn-np:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_assertion
;
np:hasProvenance
dgn-np:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_assertion
a
np:Assertion
.
dgn-np:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_provenance
a
np:Provenance
.
dgn-np:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_assertion
{
miriam-gene:4566
a
ncit:C16612
.
lld:C0001125
a
ncit:C7057
.
dgn-gda:DGNfea7ef13aeedb3223e4a68a561ac08e8
sio:SIO_000628
miriam-gene:4566
,
lld:C0001125
;
a
sio:SIO_001121
.
}
dgn-np:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_provenance
{
dgn-np:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_assertion
dcterms:description
"[Examination of DNA from the affected sibs showed no deletions in the mitochondrial DNA nor the mutations identified in the syndromes of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) or myoclonus, and epilepsy associated with rugged-red fibers (MERRF).]. 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:7726239
;
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:NP871936.RAl8cYejhtCmsnUb7V1PBhC0B0DPHPJ961-BeAqtCGnQQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:53+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" .
}