@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4
> .
@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:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_head
{
this:
np:hasAssertion
dgn-np:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_assertion
;
np:hasProvenance
dgn-np:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_provenance
;
np:hasPublicationInfo
dgn-np:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_assertion
a
np:Assertion
.
dgn-np:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_provenance
a
np:Provenance
.
dgn-np:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_assertion
{
miriam-gene:6390
a
ncit:C16612
.
lld:C0023520
a
ncit:C7057
.
dgn-gda:DGNa46375c7d848599c63a25a9d8886ed93
sio:SIO_000628
miriam-gene:6390
,
lld:C0023520
;
a
sio:SIO_001121
.
}
dgn-np:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_provenance
{
dgn-np:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_assertion
dcterms:description
"[In addition, congenital complex II deficiencies due to inherited homozygous mutations of the catalytic components of complex II (SDHA and SDHB) and the SDHAF1 assembly factor lead to childhood disease including Leigh syndrome, cardiomyopathy and infantile leukodystrophies.]. 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:23174333
;
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:NP688767.RAaH6zBF8abzlITQBdeSlRBwTPD5nKyk0a6SVKnWJ3pK4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:35+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" .
}