@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_head
{
this:
np:hasAssertion
dgn-np:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_assertion
;
np:hasProvenance
dgn-np:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_provenance
;
np:hasPublicationInfo
dgn-np:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_assertion
a
np:Assertion
.
dgn-np:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_provenance
a
np:Provenance
.
dgn-np:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_assertion
{
miriam-gene:5428
a
ncit:C16612
.
lld:C0085215
a
ncit:C7057
.
dgn-gda:DGN7665b8cdf517f9bf826ae01fd68dfaa7
sio:SIO_000628
miriam-gene:5428
,
lld:C0085215
;
a
sio:SIO_001122
.
}
dgn-np:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_provenance
{
dgn-np:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_assertion
dcterms:description
"[The clinical features of the patient are the most important features to select putative POLG mutation carriers and not the presence of mtDNA deletions or OXPHOS (oxidative phosphorylation) activity. The authors conclude that POLG mutations are an importan]. 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:19578034
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP128139.RA-43EbbAFZITeee03jn6MlzxuYd7HnhZ_2_6veO-Gh10130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:52+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}