@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I
> .
@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:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_head
{
this:
np:hasAssertion
dgn-np:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_assertion
;
np:hasProvenance
dgn-np:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_provenance
;
np:hasPublicationInfo
dgn-np:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_assertion
a
np:Assertion
.
dgn-np:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_provenance
a
np:Provenance
.
dgn-np:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_assertion
{
miriam-gene:56652
a
ncit:C16612
.
lld:C0029124
a
ncit:C7057
.
dgn-gda:DGN7577c70a6f6d18f9630b10e89ee790d8
sio:SIO_000628
miriam-gene:56652
,
lld:C0029124
;
a
sio:SIO_001122
.
}
dgn-np:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_provenance
{
dgn-np:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_assertion
dcterms:description
"[The clinical findings in this patient indicate that the combination of the two mtDNA mutations resulted in the expected combined phenotype since the mtDNA deletion mutation accounted for the PEO and the mtDNA G11778A point mutation for the optic atrophy.]. 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:19015050
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP923814.RAVu2hzxFq9ICKQp1a5et6O7fn5ll3UoYBvaO1g-DTw0I130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:04+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" .
}