@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ
> .
@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:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_head
{
this:
np:hasAssertion
dgn-np:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_assertion
;
np:hasProvenance
dgn-np:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_assertion
a
np:Assertion
.
dgn-np:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_provenance
a
np:Provenance
.
dgn-np:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_assertion
{
miriam-gene:10993
a
ncit:C16612
.
lld:C0030421
a
ncit:C7057
.
dgn-gda:DGN87b095f8517a48632b0c5d767ca9626c
sio:SIO_000628
miriam-gene:10993
,
lld:C0030421
;
a
sio:SIO_001121
.
}
dgn-np:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_provenance
{
dgn-np:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_assertion
dcterms:description
"[PGL is caused by germ line heterozygous inactivating mutations in the SDHB (PGL4), SDHC (PGL3), or SDHD (PGL1) genes, which encode three of the four subunits of mitochondrial complex II (succinate dehydrogenase; SDH).]. 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:15264276
;
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:NP299766.RAUWvkzqPLvSpejUJA2LVgIPKPASN0gIRL3EnVN7yu-GQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}