@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo
> .
@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:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_head
{
this:
np:hasAssertion
dgn-np:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_assertion
;
np:hasProvenance
dgn-np:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_provenance
;
np:hasPublicationInfo
dgn-np:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_assertion
a
np:Assertion
.
dgn-np:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_provenance
a
np:Provenance
.
dgn-np:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_assertion
{
miriam-gene:5428
a
ncit:C16612
.
lld:C1850303
a
ncit:C7057
.
dgn-gda:DGN536d635e3a29fb9f0e57c4ffea7c5586
sio:SIO_000628
miriam-gene:5428
,
lld:C1850303
;
a
sio:SIO_001121
.
}
dgn-np:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_provenance
{
dgn-np:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_assertion
dcterms:description
"[Autosomal recessive progressive external ophthalmoplegia (PEO) is one clinical disorder associated with multiple mitochondrial DNA deletions and can be caused by missense mutations in POLG, the gene encoding the mitochondrial DNA polymerase gamma.]. 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:12825077
;
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:NP871078.RAlWRGUMGwqtV9_8mpH5pi9IMpl3uvXp095u5wpUifrCo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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: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" .
}