@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs
> .
@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:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_head
{
this:
np:hasAssertion
dgn-np:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_assertion
;
np:hasProvenance
dgn-np:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_provenance
;
np:hasPublicationInfo
dgn-np:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_assertion
a
np:Assertion
.
dgn-np:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_provenance
a
np:Provenance
.
dgn-np:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_assertion
{
miriam-gene:8050
a
ncit:C16612
.
lld:C0034345
a
ncit:C7057
.
dgn-gda:DGNed03ec975076e47a96843925432209a7
sio:SIO_000628
miriam-gene:8050
,
lld:C0034345
;
a
sio:SIO_001121
.
}
dgn-np:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_provenance
{
dgn-np:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_assertion
dcterms:description
"[Mutations in the genes for the other subunits have all been described, but only dihydrolipoamide dehydrogenase (E3) and E3 binding protein (E3BP) defects contribute significantly to the total number of patients with PDH deficiency.]. 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:16904023
;
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:NP372029.RAhlbaAHCJ6BqmafBHsdWFMXnlkQhaXZWbuhrg65eG6Zs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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" .
}