@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk
> .
@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:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_head
{
this:
np:hasAssertion
dgn-np:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_assertion
;
np:hasProvenance
dgn-np:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_provenance
;
np:hasPublicationInfo
dgn-np:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_assertion
a
np:Assertion
.
dgn-np:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_provenance
a
np:Provenance
.
dgn-np:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_assertion
{
miriam-gene:1351
a
ncit:C16612
.
lld:C0162671
a
ncit:C7057
.
dgn-gda:DGNc496244e25fdb962c6cade1da7568f43
sio:SIO_000628
miriam-gene:1351
,
lld:C0162671
;
a
sio:SIO_001121
.
}
dgn-np:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_provenance
{
dgn-np:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_assertion
dcterms:description
"[We also describe systemic manifestations of MELAS-associated mutations, including cardiac, renal, endocrine, gastrointestinal, and endothelial abnormalities and pathology, as well as the hypothetical role of derangements to COX enzymatic function in driving the unique pathology and clinical manifestations of 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:18990125
;
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:NP845666.RAuMHhhcH2g7s-TgOQ05IdzhSqb_9Q6cW8_cowz--eGIk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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" .
}