@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI
> .
@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:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_head
{
this:
np:hasAssertion
dgn-np:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_assertion
;
np:hasProvenance
dgn-np:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_provenance
;
np:hasPublicationInfo
dgn-np:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_assertion
a
np:Assertion
.
dgn-np:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_provenance
a
np:Provenance
.
dgn-np:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_assertion
{
miriam-gene:617
a
ncit:C16612
.
lld:C1864002
a
ncit:C7057
.
dgn-gda:DGN117d6fb4f2893d325dbd8c386230ba68
sio:SIO_000628
miriam-gene:617
,
lld:C1864002
;
a
sio:SIO_001121
.
}
dgn-np:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_provenance
{
dgn-np:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_assertion
dcterms:description
"[Interestingly, the British and Turkish patients had complex III deficiency, whereas in the Finnish patients with GRACILE syndrome complex III activity was within the normal range, implying that BCS1L has another cellular function that is uncharacterized but essential and is putatively involved in iron metabolism.]. 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:12215968
;
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:NP874715.RAut5Q6F2mIoenqZBe9nyiNkxobHFMIrp_LqfUjGSfWtI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}