@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI
> .
@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:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_head
{
this:
np:hasAssertion
dgn-np:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_assertion
;
np:hasProvenance
dgn-np:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_provenance
;
np:hasPublicationInfo
dgn-np:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_assertion
a
np:Assertion
.
dgn-np:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_provenance
a
np:Provenance
.
dgn-np:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_assertion
{
miriam-gene:23451
a
ncit:C16612
.
lld:C0342782
a
ncit:C7057
.
dgn-gda:DGN655c6ba40c82e074c59df6aec9a846cf
sio:SIO_000628
miriam-gene:23451
,
lld:C0342782
;
a
sio:SIO_001121
.
}
dgn-np:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_provenance
{
dgn-np:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_assertion
dcterms:description
"[We sequenced the PPA2 gene in 13 patients with mitochondrial DNA depletion syndromes (MDS) of unknown cause to determine if mutations in the PPA2 gene of these patients were associated with this disease.]. 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:16300924
;
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:NP809279.RA0LoaPVh1_HdORxGcJi6WH6kDPFrgmDS44HyGfxrkhFI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}